Primary Device ID | 00880304220195 |
NIH Device Record Key | 25792372-28df-468d-a2f0-5b4365122702 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEXLOC MODULAR HIP SYSTEM |
Version Model Number | 12-104354 |
Catalog Number | 12-104354 |
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 | 00880304220195 [Primary] |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
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 |
00880304220195 | 12-104354 |
00880304220188 | 12-104353 |
00880304220171 | 12-104352 |
00880304220164 | 12-104349 |
00880304220157 | 12-104348 |
00880304220140 | 12-104345 |
00880304220096 | 12-104318 |
00880304220089 | 12-104317 |
00880304220072 | 12-104316 |
00880304220058 | 12-104310 |
00880304220041 | 12-104309 |
00880304220034 | 12-104308 |
00880304220027 | 12-104305 |
00880304220010 | 12-104303 |
00880304220003 | 12-104301 |
00880304011144 | 12-104347 |
00880304007543 | 12-104346 |
00880304002159 | 12-104304 |
00880304000681 | 12-104302 |