Primary Device ID | 10850015055628 |
NIH Device Record Key | 4d195169-07c1-415e-9b7a-0e01c70601c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WOUND CARE TREATMENT PACK |
Version Model Number | S-25619 |
Company DUNS | 039612668 |
Company Name | ULINE, 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 | true |
Device Combination Product | true |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |