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";s:4:"text";s:8437:"Medtronic, Inc., registered in the U.S. and other countries. GeoSurgical™   |  Global Distributor Since 2003. Numeric value for the clinically relevant size measurement of the medical device. See 21 CFR 807.3(b) for exceptions. Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English. The version or model identifies all devices that have specifications, performance, size, and composition within limits set by the labeler. Product images are for display only. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. View and Download Medtronic 3537 programming manual online. Seller assumes all responsibility for this listing. Dimension type for the clinically relevant measurement of the medical device. Product images are for display only. We respond to notices of alleged copyright infringement and terminate accounts of repeat infringers The information will be sent to a third-party site. Additional undefined device size not represented in the GUDID Size Type LOV. Medtronic Bladder Control Therapy A video of how the InterStim II system electrically stimulates the sacral nerve for bladder control therapy. This kit contains 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction. West Coast Medical Resources, LLC. Indicates that the device or packaging contains natural rubber that contacts humans as described under 21 CFR 801.437. Not sold to individuals. “WestCMR” and “WestCMR Surgical Surplus Marketplace” are trademarks of medtronic interstim test lead: test simulation lead kit and test simulation lead. about submitting notices and www.HIPAASpace.com policy about responding to notices in our Help Center. Classification for devices issued by the FDA. As with most medical facilities, please call for an appointment before visiting. All products sold by WestCMR are in-date. Submitting this form will take you off of DOTmed.com. in-stock orders received before 4pm est shipped same day. Indicates the high value for storage and handling requirements. Choose the best InterStim™ system for each patient. Enjoy the benefits of The World's Leading New & Used Medical Equipment Marketplace. Both systems are full-body* MRI eligible and deliver the same therapy with long-term relief. Indicates the date this particular package configuration is discontinued by the labeler. Global Unique Device ID: 00613994572042. medtronic 3057: each. Not sold to individuals. All rights reserved. Device Name: LEAD 3057-1SC TEST SCREENER 1PK US BOWEL. We provide information to help copyright holders manage their intellectual property online. All products sold by WestCMR are in-date. 3537 Controller pdf manual download. Doctor Telephone Nurse Hotline Clinic Hospital © 1997-2020 WestCMR. Not sold to individuals. Please see the ASTM F2503-13 standard for more information. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The number of packages with the same Primary DI or Package DI within a given packaging configuration. Instructions for Downloading Viewers and Players. The suction devices are part of a family of reusable ENT instrument... Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. Th... 2 08/21/2017 Medtronic Navigation, Inc. Z-3054-2017 - Medtronic Suction 9734308 Small AxiEM ENT, reusable, Rx. The Donation Identification Number is applicable to devices that are also regulated as HCT/Ps and is a number that is assigned to each donation. Medtronic Finland Oy Kaikki oikeudet pidätetään Lentäjäntie 3, 01530 Vantaa, Suomi Finland. MUINA AIKOINA KIIREELLISISSÄ ASIOISSA JÄTÄ VIESTI JA SOITAMME SINULLE TAKAISIN. Click here to see the Equipment Listings similar to 'MEDTRONIC 3057 Test Stimulation Lead' on DOTmed, STACKHOUSE 24187 Microtek Tubing For Sale, DAVOL Salute Removal Device 0113026 , Laparoscopy For Sale, DORC 23G x 0.6mm Vertical Microscissors Forcep 1286.E06 w/ Case For Sale, Access and use of this site is subject to the terms and conditions of our. Medtronic Home Page: This site is being updated continuously as more information becomes available. © 1997-2020 WestCMR. If you think somebody is violating your copyrights and want to notify us, you can find information 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 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). Organization accredited by FDA to operate a system for the issuance of UDIs. This kit includes Kit 9733452 (containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). This information may 1) be on a label attached to a durable device, 2) be on a package of a disposable device, or 3) appear in labeling materials of an implantable device. Instructions for Downloading Viewers and Players. Product images are for display only. WestCMR does not represent or claim any relationship to the respective companies or their equipment or products, names are used for reference only. The catalog, reference, or product number found on the device label or accompanying packaging to identify a particular product. Indicates the method(s) of sterilization that can be used for this device prior to device use on the patient. for InterStim Therapy. Indicates that the device is intended for one use or on a single patient during a single procedure. Product images are for display only. Name of the common device type associated with the GMDN Preferred Term Code/FDA PT Code. Need Help? 9734378, reusable, RX. HIPAA liability, trademark, document use and software licensing rules apply. Indicates whether the package is in commercial distribution as defined under 21 CFR 807.3(b). Medtronic's medical therapies treat cardiac and vascular diseases, diabetes, and neurological and musculoskeletal conditions. All rights reserved. in-stock orders received before 4pm est shipped same day. All Trademarks & Logos belong to their respective owners. Indicates whether the device is in commercial distribution as defined under 21 CFR 807.3(b). Indicates that natural rubber latex was not used as materials in the manufacture of the medical product and container and the device labeling contains this information. INTERSTIM WITHOUT LIMITS™ Your best choice for sacral neuromodulation. Indicates the medical device is free from viable microorganisms. The device is exempt from Direct Marking requirements under 21 CFR 801.45. This date 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. “WestCMR” and “WestCMR Surgical Surplus Marketplace” are trademarks of Percutaneous screening was performed with a helical percutaneous electrode designed to resist dislodgement (Medtronic 3057), which was an initial problem. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. 0800 164 064 Indicates the low value for storage and handling requirements. Number of medical devices in the base package. medtronic interstim test lead: test simulation lead kit and test simulation lead. RX only. Copyright © 2007-2020. medtronic 1514000: each. If you do not find a clinic near your location, please see the Frequently Asked Questions. 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.) Indicates the date the DI Record is published and available via Public Search. 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