Primary Device ID | 00880304672239 |
NIH Device Record Key | f664a912-3e41-450e-b869-d8bcf2f74ca3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G7 FINNED ACETABULAR SHELL |
Version Model Number | 110017116 |
Catalog Number | 110017116 |
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 | 00880304672239 [Primary] |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-08 |
Device Publish Date | 2020-04-30 |
00880304672185 | 110017111 |
00880304672178 | 110017110 |
00880304672161 | 110017109 |
00880304672154 | 110017108 |
00880304672147 | 110017107 |
00880304672130 | 110017106 |
00880304672123 | 110017105 |
00880304672116 | 110017104 |
00880304672109 | 110017103 |
00880304672093 | 110017102 |
00880304672086 | 110017101 |
00880304672079 | 110017100 |
00880304672062 | 110017099 |
00880304672055 | 110017098 |
00880304672246 | 110017117 |
00880304672239 | 110017116 |
00880304672222 | 110017115 |
00880304672215 | 110017114 |
00880304672208 | 110017113 |
00880304672192 | 110017112 |