Primary Device ID | 07640187461442 |
NIH Device Record Key | a825aacd-c353-4183-a993-96eb9f876985 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRIFT 3.5mm 1/3 Tubular Plate, 13 Hole |
Version Model Number | B-210013 |
Company DUNS | 480244832 |
Company Name | Bonebridge AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
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 |