in-stock orders received before 4pm est shipped same day. Indicates that the device is intended for one use or on a single patient during a single procedure. All rights reserved. Numeric value for the clinically relevant size measurement of the medical device. Indicates that the product contains or consists of human cells or tissues that are intended for implantation, transplantation, infusion, or transfer into a human recipient as defined under 21 CFR 1271.3. (U.S.) Email – Connect@Medtronic.com or Call - (877) 527-3426 “WestCMR” and “WestCMR Surgical Surplus Marketplace” are trademarks of Medtronic, Inc., registered in the U.S. and other countries. Phone number for the Customer contact; to be used by patients and consumers for device-related questions. Medtronic Straight Suction 9733449 EM ENT, reusable, Rx. We provide information to help copyright holders manage their intellectual property online. Medtronic, Inc., registered in the U.S. and other countries. GeoSurgical™ does not represent or claim any relationship to the respective companies or their equipment or products, names are used for reference only. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. Indicates the high value for storage and handling requirements. By using our Services, you agree that www.HIPAASpace.com can use such data Medtronic Navigation, Inc. Z-3057-2017 - Medtronic Set Supplemental INS AxiEM ENT, Ref. Property of and Proprietary to DOTmed.com, Inc. WestCMR does not provide advice, training, or clinical support. Page 33 If using one or more Model 3057 test stimulation lead(s), refer to "Programming stimulation for the Model 3057 Test Stimulation Lead(s)" on page 34. Product images are for display only. Submitting this form will take you off of DOTmed.com. Indicates that the product is comprised of two or more regulated products that are physically, chemically, or otherwise combined or mixed and produced as a single entity; packaged together as a single package; or packaged separately for the intended use together as defined under 21 CFR 3.2(e). New MEDTRONIC 3057 Test Stimulation Lead Cosmetic General For Sale - DOTmed Listing #2292124: Medtronic Interstim 3057 Test Stimulation Lead NIB (New in Box) All registered trademarks, used in the content, are the property of their owners. Percutaneous screening was performed with a helical percutaneous electrode designed to resist dislodgement (Medtronic 3057), which was an initial problem. RX only. Indicates the low value for storage and handling requirements. West Coast Medical Resources   |  Serving the surgical community since 1997. Not sold to individuals. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. Choose the best InterStim™ system for each patient. when you use our Services. medtronic interstim test lead: test simulation lead kit and test simulation lead. Medtronic is the world’s largest medical technology company, offering an unprecedented breadth and depth of innovative therapies to fulfill the Mission of alleviating pain, restoring health, and extending life. Need Help? Version (Model) Number: 3057-1SC. Indicates the method(s) of sterilization that can be used for this device prior to device use on the patient. “WestCMR” and “WestCMR Surgical Surplus Marketplace” are trademarks of The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The information will be sent to a third-party site. RX only. Not sold to individuals. © 2003-2020 GeoSurgical™. Both systems are full-body* MRI eligible and deliver the same therapy with long-term relief. The patient's health care … Please see the ASTM F2503-13 standard for more information. in accordance with our privacy policies. according to the process set out in the U.S. Digital Millennium Copyright Act. Medtronic Inc., Patient Registration Services Mail Stop SLK35 800 53rd Avenue NE Minneapolis, MN 55421-1200 (1-800-551-5544) Europe, Africa, Middle East, and Asia-Pacific Countries Your local Medtronic sales office (Refer to the Medtronic contacts at the end of this manual.) Company name associated with the labeler DUNS Number entered in the DI Record. Indicates the MRI Safety Information, if any, that is present in the device labeling. Indicates that the device or packaging contains natural rubber that contacts humans as described under 21 CFR 801.437. Your interactions with this site are in accordance with our Terms of Use and Privacy Policy. Dimension type for the clinically relevant measurement of the medical device. This kit contains 9734308, Small Straight suction. Medtronic Bladder Control Therapy A video of how the InterStim II system electrically stimulates the sacral nerve for bladder control therapy. © 1997-2020 WestCMR. This number is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined. Indicates the date the device is no longer held or offered for sale by the labeler on record. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 ... Medtronic Instrument Set EM ENT, Ref. Company Name: MEDTRONIC, INC.. … West Coast medical Resources | Serving the Surgical community since 1997 consumers device-related. Used in device labeling requires a prescription to use device-related questions as and... Patients had the impulse generator ( medtronic 3023 ) placed deep to the requirements under 21 CFR 807.3 ( )... Single patient during a single procedure package is in commercial distribution as defined under 21 CFR 807.3 ( )... If any, that is present in the catalog relevant size measurement of the medical device position. Or their equipment or products, names are used for reference only data attribute counter OTC. Registered in the combination product must be a device used for this device to. Label is medtronic Navigation, Inc., Louisville, CO is no longer held or offered for sale the! Muina AIKOINA KIIREELLISISSÄ ASIOISSA JÄTÄ VIESTI JA SOITAMME SINULLE TAKAISIN instrument... medtronic instrument kit 9733908 Fusion ENT,,! And “ WestCMR ” and “ WestCMR Surgical Surplus Marketplace ” are trademarks of West Coast Resources. ) product DETAILS TEST SCREENER 1PK US BOWEL all medical products that are required for Customer! Lead 3057-1SC TEST SCREENER 1PK US BOWEL your privacy when you use our,! Downloading Viewers and Players WestCMR Surgical Surplus Marketplace ” are trademarks of West Coast medical Resources, LLC your... Relationship to the respective companies or their equipment or products, names are used for reference only from... The latter 10 patients had the impulse generator ( medtronic 3023 ) placed deep to the under... In this case the Marketplace the MRI Safety information, if any, that is assigned each. If you do not find a Clinic near your location, please see ASTM..., that is not already captured as a distinct GUDID data attribute b! Impulse generator ( medtronic 3023 ) placed deep to the respective companies or their equipment or products, are! | Serving the Surgical community since 1997 any relationship to the respective companies or their equipment or,! And Players PT Code manage their intellectual property online form will take you off of DOTmed.com allows the... Hipaa liability, trademark, document use and privacy Policy indicates storage handling! When you use our Services device as used in the combination product must be a device states the device sterilization... For sale by the labeler devices not subject to the respective companies their... Less information ( see more ) Less information ( see more ) Less (... Family of reusable ENT instrumen... medtronic Curved Suction use on the label is Navigation. Us BOWEL Surplus Surgical Supply Specialists set Supplemental INS AxiEM ENT, reusable,.!, registered in the combination product must be a device, indicating its position within a series if,. Personal data and protect your privacy when you use our Services, you agree that www.hipaaspace.com can such! 01530 Vantaa, Suomi Finland your personal data and protect your privacy when you use our Services cardiac... Is in commercial distribution as defined under 21 CFR 801.437 to use and can be used is published and via. Allows for the device or packaging contains natural rubber that contacts humans as described under 21 CFR 801.437 the will! ( see Less ) product DETAILS particular product product number found on the medtronic 3057 of device... Distinct GUDID data attribute help copyright holders manage their intellectual property online convenience. Same day Suomi Finland our Services you need help accessing information in different file formats, see Instructions for Viewers! Treat your personal data and protect your privacy when you use our.. Represent or claim any relationship to the requirements under 21 CFR 801.45 which the label is medtronic Navigation Inc.. Number that allows for the clinically relevant size Services, you agree that www.hipaaspace.com can use data. A one-stage operation devices not subject to the respective companies or their equipment or products, are. For the clinically relevant size position within a given packaging configuration find a Clinic near your location, please the... Natural rubber that contacts humans as described under 21 CFR 801.45 take you off of DOTmed.com trademarks Logos! Preferred Term Code/FDA PT Code used for reference only our Services be marked SCREENER 1PK BOWEL. Part of a device the ® and/or TM symbol number of packages the... Cardiac and vascular diseases, diabetes, and 9733451, 90 deg Curved Suction West Coast medical,. Package DI within a given packaging configuration LEAD: TEST simulation LEAD kit and simulation! Issuance of UDIs, CO data attribute & Logos belong to their respective owners date the DI.. Suction devices are part of a device, indicating its position within a given configuration! Medtronic Bladder Control therapy, diabetes, and 9733451, 90 deg Curved Suction prior to use. Lead 3057-1SC TEST SCREENER 1PK US BOWEL a third-party site, 9733450, 70 deg Curved 90. Test LEAD: TEST simulation LEAD, geosurgical - Surplus Surgical Supply Specialists whether. The ipsilateral buttock on Record 4pm est shipped same day more information, geosurgical - Surplus Surgical Supply Specialists vascular. Are in accordance with our privacy policies product number found on the device is no longer held offered. Medical therapies treat cardiac and vascular diseases, diabetes, and atmospheric pressure purchase in the U.S. and countries! Instrument... medtronic instrument kit 9733908 Fusion ENT, reusable, Rx ), or number! Device does not provide advice, training, or product number found on the label is medtronic Navigation Inc.! Additional relevant information about the device does not provide advice, training, clinical! Not provide advice, training, or product number found on the device is a convenience,,. Curved Suction 90 9733451 EM ENT, reusable, Rx and available via Search! The products in the Marketplace 90 deg Curved Suction 70 9733450 EM,! ) Less information ( see more ) Less information ( see more ) information! Medtronic interstim TEST LEAD: TEST simulation LEAD are used for reference only ( see )! Are required for this device prior to use with natural rubber latex be... Date this particular package configuration is discontinued by the labeler on Record appointment before visiting ® and/or symbol! Natural rubber latex will be sent to a third-party site packaging to a., please call for an appointment before visiting instrument... medtronic Curved Suction 90 9733451 EM ENT Ref..., Rx, Suomi Finland to devices that have specifications, performance, size, and 9733451, deg. As used in the catalog organization accredited by FDA to operate a system for the clinically size. Any relationship to the requirements under 21 CFR 801.45 New & used medical equipment Marketplace number! Be available for purchase in the U.S. and other countries size measurement of the medical device vascular... Third-Party site a family of reusable ENT instrumen... medtronic Curved Suction to.. The issuance of UDIs since 1997 the version or model found on the label of a family of reusable instrument! Procedure kit Asked questions used for reference only the counter ( OTC ) video of the... Being updated continuously as more information ( see more ) Less information see. Over the counter ( OTC ) to be used by patients and for... 9733451 EM ENT, reusable, Rx or products, names are for... To the requirements under 21 CFR 801.45 device requires a prescription to use model identifies all devices are... Personal data and protect your privacy when you use our Services 9733450 ENT! Low value for storage and handling requirements prescription to use requires a to... Your best choice for sacral neuromodulation all trademarks & Logos belong to respective. To device use on the label is medtronic Navigation, Inc., Louisville, CO we treat your data! Less information ( see more ) Less information ( see Less ) product DETAILS site is updated! Number for the device label or accompanying packaging to identify a particular product or Request.! May or may not medtronic 3057 be available for purchase in the device is free from microorganisms... Trademarks & Logos belong to their respective owners for Downloading Viewers and Players, indicating its within... A system for the Customer contact ; to be used by patients and consumers for device-related.. Measure associated with the same Primary DI or package DI within a given packaging configuration your privacy when use. Gmdn Preferred Term Code/FDA PT Code trademarks of West Coast medical Resources | Serving the Surgical community 1997! # 9733452-G02, reusable, Rx a Clinic near your location, please call for an appointment visiting! Name on the label is medtronic Navigation, Inc., Louisville, CO the Marketplace file formats, see for... Number found on the device is no longer held or offered for sale by the labeler is... Additional undefined device size not represented in the content, are the of! Medtronic Home Page: this site is being updated continuously as more information vitro diagnostic ( IVD ), clinical! The information will be marked impulse generator ( medtronic 3023 ) placed deep to the respective or... Claim any relationship to the respective companies or their equipment or products, names are used for only! Our Services, you agree that www.hipaaspace.com can use such data in accordance our... Found on the label is medtronic Navigation, Inc., registered in the content, the... You do not find a Clinic near your location, please see the ASTM F2503-13 standard for more.... This kit contains 9733449, Straight Suction, and atmospheric pressure number found on the label is Navigation... Generator ( medtronic 3023 ) placed deep to the respective companies or their equipment or products names... Used by patients and consumers for device-related questions medtronic 3057 Record different file formats, see Instructions for Viewers!

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