Primary Device ID | 07640149886542 |
NIH Device Record Key | ef978d25-c96f-43b2-9a35-7e0bfd00754c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRI |
Version Model Number | A |
Catalog Number | TLM-47-08-P45 |
Company DUNS | 485821164 |
Company Name | TRI Dental Implants Int. AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |