Primary Device ID | 03700386933769 |
NIH Device Record Key | c3e8a4df-ec71-4d3a-992b-0b06d2234372 |
Commercial Distribution Discontinuation | 2017-11-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | HLS KNEETEC |
Version Model Number | GDI094 |
Company DUNS | 260324876 |
Company Name | TORNIER |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +330476613500 |
order@tornier.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700386933769 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2015-10-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HLS KNEETEC 77617668 3688507 Live/Registered |
CORIN LIMITED 2008-11-19 |