Primary Device ID | 00887868083129 |
NIH Device Record Key | d530ced9-1f2d-4e00-a2c9-20b3028f8972 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MINI DOUBLE TIPPED GUIDE WIRE |
Version Model Number | 04866 |
Catalog Number | 04866 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 5 |
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 | 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 |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868083129 [Primary] |
GS1 | 70887868083128 [Unit of Use] |
HTY | PIN, FIXATION, SMOOTH |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868083129]
Moist Heat or Steam Sterilization
[00887868083129]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-22 |
00887868004087 - PRIMARY TREPHINE | 2024-04-03 |
00887868004094 - BUSHING | 2024-04-03 |
00887868004100 - SECONDARY TREPHINE | 2024-04-03 |
00887868048272 - TREPHINE | 2024-04-03 |
00887868048289 - TREPHINE | 2024-04-03 |
00887868048296 - TREPHINE | 2024-04-03 |
00887868048302 - TREPHINE | 2024-04-03 |
00880304658387 - Compress® | 2024-03-11 |