Primary Device ID | B239B2501 |
NIH Device Record Key | d7be7a9a-7356-440d-9f5c-9661bfabecbb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wound Measuring Guide |
Version Model Number | B250 |
Catalog Number | B250 |
Company DUNS | 024113805 |
Company Name | TRADEMARK MEDICAL, L.L.C. |
Device Count | 250 |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B239B2500 [Unit of Use] |
HIBCC | B239B2501 [Primary] |
FTY | Tape, Measuring, Rulers And Calipers |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-18 |
Device Publish Date | 2019-03-08 |
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