| Primary Device ID | 08522650086002 |
| NIH Device Record Key | 4dcb05e1-6b26-49c0-b6ad-6cf304111a14 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kitchmart |
| Version Model Number | GNN.L10B |
| 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 | 08522650085708 [Primary] |
| GS1 | 08522650086002 [Package] Contains: 08522650085708 Package: [10 Units] In Commercial Distribution |
| GS1 | 18522650085705 [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 |