Primary Device ID | 08033390066525 |
NIH Device Record Key | c8489936-c585-4030-9bb8-61415d203e89 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | C2 Hip |
Version Model Number | 9045.12.010 |
Catalog Number | 9045.12.010 |
Company DUNS | 432066322 |
Company Name | LIMACORPORATE SPA |
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 | 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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08033390066525 [Primary] |
LWJ | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08033390066525]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-07-05 |
Device Publish Date | 2018-03-13 |
08033390071673 | M8 Stem Beater-Extractor |
08033390071666 | C2 Hip - Lateralized Trial Neck |
08033390071659 | C2 Hip - Trial Neck |
08033390066594 | C2 Hip - Broach # 6 |
08033390066556 | C2 Hip - Broach # 2 |
08033390066549 | C2 Hip - Broach # 1 |
08033390066532 | C2 Hip - Broach # 0 |
08033390066525 | C2 Hip - Broach # 01 |
08033390066655 | C2 Hip - Broach # 12 |
08033390066648 | C2 Hip - Broach # 11 |
08033390066631 | C2 Hip - Broach # 10 |
08033390066624 | C2 Hip - Broach # 9 |