Primary Device ID | D7700886153 |
NIH Device Record Key | 9f435b9d-49a3-432d-bd37-0fe3bbfeef91 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCREW M2 FOR RIP.ABUTMENT |
Version Model Number | A-TG-VABUR-W-10 |
Catalog Number | A-TG-VABUR-W-10 |
Company DUNS | 433815198 |
Company Name | SWEDEN & MARTINA SPA |
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 | 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 |