Primary Device ID | 00860007935503 |
NIH Device Record Key | 8baba68f-6d43-4b90-8cc5-26ae85fe1c1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vitalin |
Version Model Number | USAW35 Medium Blue |
Company DUNS | 118443347 |
Company Name | Vitalin LLC |
Device Count | 100 |
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 | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850038171070 [Unit of Use] |
GS1 | 00860007935503 [Primary] |
LZA | Polymer Patient Examination Glove |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-23 |
Device Publish Date | 2022-05-13 |
00860007935503 | Nitrile medical exam gloves 3.5 mil Blue |
00860007935534 | Nitrile medical exam gloves 3.5 Blue |
00860007935527 | Nitrile medical exam gloves 3.5 mil Blue |
00860007935510 | Nitrile medical exam gloves 3.5 mil Blue |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() VITALIN 73776277 1604294 Dead/Cancelled |
CARDINAL LABORATORIES, INC. 1989-01-23 |