Primary Device ID | 08522650085944 |
NIH Device Record Key | 31512d05-da3d-41c2-830f-92e50666279a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kitchmart |
Version Model Number | GNN.M10B |
Company DUNS | 030905836 |
Company Name | Kitchmart Trading |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08522650085630 [Primary] |
GS1 | 08522650085944 [Package] Contains: 08522650085630 Package: [10 Units] In Commercial Distribution |
GS1 | 18522650085637 [Unit of Use] |
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 | 2023-02-20 |
Device Publish Date | 2023-02-12 |
09557621701683 | GNN.XL100 |
09557621701584 | GNN.L100 |
09557621701577 | GNN.M100 |
08522650086170 | GNN.XL10B |
08522650086002 | GNN.L10B |
08522650085944 | GNN.M10B |
10852265008980 | GNN.S10B |
00852265008617 | GNN.XL10B |
00852265008600 | GNN.L10B |
00852265008563 | GNN.M10B |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KITCHMART 77226571 3394587 Live/Registered |
KITCHMART TRADING CORP 2007-07-11 |