| Primary Device ID | 00852265008600 | 
| NIH Device Record Key | d42f46e6-7578-42e1-9446-a557eefbcd5a | 
| 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 | true | 
| 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 | 00852265008570 [Primary] | 
| GS1 | 00852265008600 [Package] Contains: 00852265008570 Package: [10 Units] In Commercial Distribution | 
| GS1 | 10852265008577 [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 | 2023-09-14 | 
| Device Publish Date | 2023-09-06 | 
| 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 |