Primary Device ID | 00850003355535 |
NIH Device Record Key | c3de247c-cec6-46cd-b313-33a98abb1e41 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medtronics |
Version Model Number | 29694 |
Catalog Number | 29694 |
Company DUNS | 014464314 |
Company Name | EXACT MEDICAL MANUFACTURING, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850003355535 [Primary] |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-08-08 |
Device Publish Date | 2019-07-31 |
10850003355549 | Sterile Drapes 9736245 Autoguide 15pk / Sterile Drapes Autoguide 15 pack, Inner case 1085000335 |
00850003355535 | DRAPE 29694 STERILE CU STEALTH AUTOGUIDE |
00850003355528 | DRAPE 31304 STERILE TU STEALTH AUTOGUIDE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDTRONICS 88812944 not registered Live/Pending |
Precision One Lifecare Limited 2020-02-27 |