Primary Device ID | 10819856020479 |
NIH Device Record Key | f3866024-3423-409b-802c-5c3f4c857d96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 1st Choice, AMMEX Professional |
Version Model Number | 1ENVPFLCS2 |
Company DUNS | 187070768 |
Company Name | AMMEX 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 | 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 | 10819856020479 [Primary] |
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 | 2023-07-06 |
Device Publish Date | 2023-06-28 |
10819856020486 | 1ENVPFXLCS2 |
10819856020479 | 1ENVPFLCS2 |
10819856020462 | 1ENVPFMCS2 |
10819856020455 | 1ENVPFSCS2 |
00819856022490 | 1ENVPFXLBX2 |
00819856022483 | 1ENVPFLBX2 |
00819856022476 | 1ENVPFMBX2 |
00819856022469 | 1ENVPFSBX2 |
10819856020448 | 1EINVPFXLCS2 |
10819856020431 | 1EINVPFLCS2 |
10819856020424 | 1EINVPFMCS2 |
10819856020417 | 1EINVPFSCS2 |
10819856020400 | 1EBNVPFXLCS2 |
10819856020387 | 1EBNVPFMCS2 |
10819856020370 | 1EBNVPFSCS2 |
00819856022575 | 1EBNVPFXLBX2 |
00819856022568 | 1EBNVPFLBX2 |
00819856022551 | 1EBNVPFMBX2 |
00819856022544 | 1EBNVPFSBX2 |
00819856022537 | 1EINVPFXLBX2 |
00819856022520 | 1EINVPFLBX2 |
00819856022513 | 1EINVPFMBX2 |
00819856022506 | 1EINVPFSBX2 |