Primary Device ID | 07640173167884 |
NIH Device Record Key | e322d7d5-e3c5-48d0-b69b-8b6d8b3e2983 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ostaPek Interbody Fusion Cage |
Version Model Number | 23.152 |
Company DUNS | 482467792 |
Company Name | coLigne AG |
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 | 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 |