Primary Device ID | 07290110721992 |
NIH Device Record Key | 344a4730-446e-4e85-90b5-eb3f3e6ab577 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRX-BA |
Version Model Number | TRX-BA 3.3-13mm |
Catalog Number | TRX-BA 3.3-13 |
Company DUNS | 600710917 |
Company Name | HI-TEC IMPLANTS LTD. |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |