Primary Device ID | 04052199602769 |
NIH Device Record Key | df664e5f-763e-492d-b75f-17aca0c1ee8a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Zetuvit P10t Plus Silicone 10x20c |
Version Model Number | 413813 |
Company DUNS | 010137511 |
Company Name | HARTMANN USA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04052199602752 [Primary] |
GS1 | 04052199602769 [Package] Contains: 04052199602752 Package: [10 Units] In Commercial Distribution |
GS1 | 04052199602776 [Package] Package: [6 Units] In Commercial Distribution |
NAC | Dressing, Wound, Hydrophilic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-13 |
Device Publish Date | 2023-03-03 |
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