| Primary Device ID | 00880304606241 |
| NIH Device Record Key | c98272ab-101d-4d5d-a814-270e63c2402e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TAPERLOC |
| Version Model Number | 31-103266 |
| Catalog Number | 31-103266 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304606241 [Primary] |
| HTR | RASP |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304606241]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2017-05-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TAPERLOC 97643546 not registered Live/Pending |
The Trustees of the Tonya R Fisher Revocable Trust 2022-10-22 |
![]() TAPERLOC 75431304 2292129 Live/Registered |
Biomet Manufacturing, LLC 1998-02-09 |
![]() TAPERLOC 74144154 1672522 Dead/Cancelled |
Biomet, Inc. 1991-03-04 |
![]() TAPERLOC 73770456 not registered Dead/Abandoned |
BIOMET, INC. 1988-12-19 |
![]() TAPERLOC 72457303 0983732 Dead/Expired |
AMSTED INDUSTRIES INCORPORATED 1973-05-14 |