| Primary Device ID | 00762935052300 |
| NIH Device Record Key | f28ed536-9339-49ee-b99f-1a50dfc9e41c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Inteplast |
| Version Model Number | NBLK003 |
| Company DUNS | 786941427 |
| Company Name | Inteplast Group Corporation |
| 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 | true |
| Expiration Date | false |
| 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 | 00762935052300 [Primary] |
| GS1 | 07629350523002 [Package] Package: INNER [100 Units] In Commercial Distribution |
| GS1 | 07629350523071 [Package] Contains: 07629350523002 Package: OUTER [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 | 2022-06-17 |
| Device Publish Date | 2022-06-09 |
| 00762935056476 | Nitrile exam grade powder free glove size XL |
| 00762935056469 | Nitrile exam grade powder free size L |
| 00762935056452 | Nitrile exam grade powder free glove size M |
| 00762935056445 | Nitrile exam grade powder free glove size S |
| 00762935052317 | Black nitrile exam grade powder free glove size XL |
| 00762935052300 | Black nitrile exam grade powder free glove size L |
| 00762935052294 | Black nitrile exam grade powder free glove size M |
| 00762935052270 | Black Nitrile exam grade powder free glove S |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() INTEPLAST 90369804 not registered Live/Pending |
Inteplast Group Corporation 2020-12-09 |
![]() INTEPLAST 90339124 not registered Live/Pending |
Inteplast Group Corporation 2020-11-24 |
![]() INTEPLAST 87009705 5036675 Live/Registered |
Inteplast Group Corporation 2016-04-21 |
![]() INTEPLAST 74359038 1853854 Live/Registered |
INTEPLAST GROUP, LTD. 1993-02-16 |