Primary Device ID | 00781311665866 |
NIH Device Record Key | 55f66eeb-f776-4b82-841b-682d3b436b1c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DERMA TUFF |
Version Model Number | 66586 |
Company DUNS | 799540588 |
Company Name | Bunzl USA Holdings LLC |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00781311665866 [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 | 2024-04-05 |
Device Publish Date | 2024-03-28 |
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