Primary Device ID | B283E2IFBOD0 |
NIH Device Record Key | 6f3eab1d-44cf-4706-8694-62c3f63f080d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRO1TEK Trauma First Aid Bleeding Control Kit-2+ P |
Version Model Number | B283E2IFBOD0 |
Company DUNS | 827067880 |
Company Name | Pro1tek |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
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 |
Phone | 2622328790 |
info@buypro1tek.com | |
Phone | 2622328790 |
info@buypro1tek.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B283E2IFBOD0 [Primary] |
OHO | First Aid Kit Without Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-26 |
Device Publish Date | 2018-09-25 |
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