Primary Device ID | M224MRD30109 |
NIH Device Record Key | 4b42b4ed-8369-4d01-9c01-37db98242410 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Inion Trinion™ |
Version Model Number | 1 |
Catalog Number | MRD-3010 |
Company DUNS | 367994657 |
Company Name | Inion Oy |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06438408004605 [Secondary] |
HIBCC | M224MRD30109 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2017-02-07 |
M224SET30029 | 10 mm (x3) meniscus screw |
M224MRD30109 | 10 mm meniscus screw |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INION TRINION 78529646 3205010 Dead/Cancelled |
INION OY 2004-12-09 |