Primary Device ID | 05056139218644 |
NIH Device Record Key | b55b6714-62aa-48db-bf1d-7aea2b3aedc0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U-KneeTec |
Version Model Number | MDF930 |
Catalog Number | MDF930 |
Company DUNS | 295437313 |
Company Name | CORIN LTD |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +330456608978 |
severine.siracusa@coringroup.c | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com | |
Phone | +330456608978 |
severine.siracusa@coringroup.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05056139218644 [Primary] |
HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER |
Steralize Prior To Use | true |
Device Is Sterile | false |
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
[05056139218644]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-28 |
Device Publish Date | 2018-08-28 |
05056139230516 | Femoral clamp |
05056139230509 | Universal handle |
05056139230493 | Handle for punch |
05056139230486 | Femoral bone punch |
05056139230479 | Protective tibial plate |
05056139230462 | Trial femoral component S4 |
05056139230455 | Trial femoral component S3 |
05056139230448 | Trial femoral component S2 |
05056139230431 | Trial femoral component S1 |
05056139230424 | Trial femoral component S0 |
05056139230417 | AO Müller saw blade |
05056139230400 | Aesculap saw blade |
05056139230394 | Stryker B saw blade |
05056139230387 | Zimmer saw blade |
05056139230370 | Pin driver quick connect |
05056139230363 | Self tapered screw Dia. 3mm L. 40mm |
05056139230356 | Self tapered screw Dia. 3mm L. 25mm |
05056139230349 | Drill bit Ø 8 x 150 mm |
05056139230332 | Spacer 11 - 17 mm |
05056139230325 | Spacer 9 - 15 mm |
05056139230318 | Extramedullary rod |
05056139230301 | Tibial resection gauge |
05056139230295 | Posterior condyle stylus |
05056139230288 | Tbial stylus |
05056139230271 | Distal cutting guide |
05056139230264 | Tibial cutting guide Lat L/Med R |
05056139230257 | Tibial cutting guide Med L/Lat R |
05056139230240 | Fin conformator S4 |
05056139230233 | Fin conformator S3 |
05056139230226 | Fin conformator S2 |
05056139230219 | Fin conformator S1 |
05056139230202 | Fin conformator S0 |
05056139230196 | Posterior condyle cutting guide S4 Med L/Lat R |
05056139230189 | Posterior condyle cutting guide S3 Med L/Lat R |
05056139230172 | Posterior condyle cutting guide S2 Med L/Lat R |
05056139230165 | Posterior condyle cutting guide S1 Med L/Lat R |
05056139230158 | Posterior condyle cutting guide S0 Med L/Lat R |
05056139230141 | Posterior condyle cutting guide S4 Lat L/Med R |
05056139230134 | Posterior condyle cutting guide S3 Lat L/Med R |
05056139230127 | Posterior condyle cutting guide S2 Lat L/Med R |
05056139230110 | Posterior condyle cutting guide S1 Lat L/Med R |
05056139230103 | Posterior condyle cutting guide S0 Lat L/Med R |
05056139230097 | Augment distal cutting guide 4 mm |
05056139230080 | Augment distal cutting guide 3 mm |
05056139230073 | Augment distal cutting guide 2 mm |
05056139230066 | Augment distal cutting guide 1 mm |
05056139230059 | Mini spacer 3 mm |
05056139230042 | Mini spacer 2 mm |
05056139230035 | Mini spacer 1 mm |
05056139225437 | Cutting pin Ø3mm x 75mm |