Primary Device ID | 10628032500175 |
NIH Device Record Key | 6dfe691a-3afc-4384-ae74-9ed124fd7267 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DOMREX™ Syringe with safety needle |
Version Model Number | 3ML 22GX1" |
Company DUNS | 242411127 |
Company Name | Domrex Pharma Inc |
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 | 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 | 00628032500178 [Primary] |
GS1 | 10628032500175 [Package] Contains: 00628032500178 Package: Case [8 Units] In Commercial Distribution |
GS1 | 90628032500171 [Unit of Use] |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-29 |
Device Publish Date | 2024-01-21 |
10628032500182 | 3ML 25GX5/8" |
10628032500175 | 3ML 22GX1" |
10628032500151 | 3ML 21G x 1'' |
10628032325105 | 3ML |
10628032125101 | 1ML |
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 |