Primary Device ID | 07630030843310 |
NIH Device Record Key | e6a26b5f-c096-4289-8957-43c768db3cf1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bipolar Heads |
Version Model Number | 25060.2241 |
Company DUNS | 488227125 |
Company Name | Medacta International SA |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630030843310 [Primary] |
KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-11-18 |
07630030843914 | Ø28x60 |
07630030843891 | Ø28x59 |
07630030843877 | Ø28x58 |
07630030843853 | Ø28x57 |
07630030843839 | Ø28x56 |
07630030843815 | Ø28x55 |
07630030843792 | Ø28x54 |
07630030843778 | Ø28x53 |
07630030843754 | Ø28x52 |
07630030843730 | Ø28x51 |
07630030843716 | Ø28x50 |
07630030843693 | Ø28x49 |
07630030843679 | Ø28x48 |
07630030843655 | Ø28x47 |
07630030843631 | Ø28x46 |
07630030843617 | Ø28x45 |
07630030843594 | Ø28x44 |
07630030843532 | Ø22x52 |
07630030843518 | Ø22x51 |
07630030843495 | Ø22x50 |
07630030843471 | Ø22x49 |
07630030843457 | Ø22x48 |
07630030843433 | Ø22x47 |
07630030843419 | Ø22x46 |
07630030843396 | Ø22x45 |
07630030843372 | Ø22x44 |
07630030843358 | Ø22x43 |
07630030843334 | Ø22x42 |
07630030843310 | Ø22x41 |
07630030843297 | Ø22x40 |