Primary Device ID | 06975101540028 |
NIH Device Record Key | c7ae7e8c-5419-4f3f-b52c-ce72467aed5d |
Commercial Distribution Discontinuation | 2056-08-18 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ZHONG LIAN |
Version Model Number | L |
Company DUNS | 526969078 |
Company Name | ANHUI ZHONG LIAN LATEX GLOVES MANUFATURING CO.,LTD. |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06975101540028 [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 | 2022-01-18 |
Device Publish Date | 2022-01-10 |
06975101540035 | nitrile, blue, XL |
06975101540028 | nitrile, blue, L |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZHONG LIAN 78328482 2910964 Live/Registered |
HERBA ENTERPRISE, INC. 2003-11-14 |