Primary Device ID | 00880304542778 |
NIH Device Record Key | 70a3e97d-a5a5-43f9-ab07-5e38ffcb880b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SIRIUS HIP SYSTEM |
Version Model Number | 51-199333 |
Catalog Number | 51-199333 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304542778 [Primary] |
KWL | Prosthesis, hip, hemi-, femoral, metal |
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 | 2015-10-24 |
00880304652125 | 51-199331 |
00880304543683 | 596046 |
00880304543676 | 596044 |
00880304543669 | 596045 |
00880304542839 | 51-199342 |
00880304542822 | 51-199352 |
00880304542815 | 51-199332 |
00880304542808 | 51-199351 |
00880304542792 | 51-199335 |
00880304542785 | 51-199343 |
00880304542778 | 51-199333 |
00880304542761 | 51-199341 |
00880304542754 | 51-199336 |
00880304542747 | 51-199337 |
00880304542723 | 51-199301 |
00880304542716 | 51-199300 |
00880304542648 | 51-199334 |