Primary Device ID | 26928965100048 |
NIH Device Record Key | 4a7f1f78-bf0a-470e-a1b6-074a4c60e81c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Annuy Powder-free Nitrile Patient Examination Glove |
Version Model Number | S |
Company DUNS | 421347466 |
Company Name | Anhui Annuy Latex Products Co.,Ltd. |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06928965100044 [Unit of Use] |
GS1 | 16928965100041 [Primary] |
GS1 | 26928965100048 [Package] Contains: 16928965100041 Package: [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 | 2021-02-03 |
Device Publish Date | 2021-01-26 |
06928965100068 | A non-sterile device made of Nitrile intended as a protective barrier when worn on the hands of |
26928965100055 | A non-sterile device made of Nitrile intended as a protective barrier when worn on the hands of |
26928965100048 | A non-sterile device made of Nitrile intended as a protective barrier when worn on the hands of |