Primary Device ID | 00843013101629 |
NIH Device Record Key | 2551b692-6b2c-43a1-aa7e-1158f5b2fccd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ventyv |
Version Model Number | Nitrile PF Exam PLUS 5.0 (Bull) M |
Catalog Number | 10320108 |
Company DUNS | 151296659 |
Company Name | SRI TRANG USA, INC. |
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 | false |
Serial Number | false |
Manufacturing Date | false |
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 | 00843013101629 [Unit of Use] |
GS1 | 00843013101681 [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 | 2022-12-09 |
Device Publish Date | 2022-12-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VENTYV 87652304 5657159 Live/Registered |
Sri Trang Gloves (Thailand) Co., Ltd. 2017-10-19 |