Primary Device ID | 00643169021419 |
NIH Device Record Key | 13d4d925-d071-46ec-9b38-2162cfbfbcfc |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 3537FA |
Company DUNS | 796986144 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169021419 [Primary] |
EZW | Stimulator, electrical, implantable, for incontinence |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-23 |
00763000951825 - NA | 2024-05-31 CUSTOM PACK SSBB12G88R STERILE SMPL |
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00763000953621 - NA | 2024-05-31 CUSTOM PACK BB11Q49R11 3/8 EC |
00763000953638 - NA | 2024-05-31 CUSTOM PACK BB12A45R1 SMALL LOOP |
00763000953645 - NA | 2024-05-31 CUSTOM PACK BB12A44R2 LRG AV LOOP |
20763000953663 - NA | 2024-05-31 CUSTOM PACK BB12G60R 2PK 2PK CHRST TBL |
00763000953676 - NA | 2024-05-31 CUSTOM PACK BB7B00R26 UW CMAG PK |