Primary Device ID | 10628032900050 |
NIH Device Record Key | dae6beef-5227-48e0-ad7f-b815a057a22d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DOMREX™ Powder-Free Nitrile Exam Gloves |
Version Model Number | XL |
Company DUNS | 242411127 |
Company Name | Domrex Pharma 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628032900053 [Primary] |
GS1 | 10628032900050 [Package] Contains: 00628032900053 Package: Case [10 Units] In Commercial Distribution |
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 | 2024-01-29 |
Device Publish Date | 2024-01-19 |
10628032900050 | XL |
10628032900043 | L |
10628032900036 | M |
10628032900029 | S |
00628032900015 | XS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DOMREX 90895179 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |
DOMREX 90895178 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |
DOMREX 90895175 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |
DOMREX 90895174 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |
DOMREX 90895173 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |
DOMREX 90895172 not registered Live/Pending |
DOMREX PHARMA INC. 2021-08-21 |