A.L.P.S.® 110008333
GUDID 00887868457869
Biomet Orthopedics, LLC
Bone lever/elevator| Primary Device ID | 00887868457869 |
| NIH Device Record Key | 1efd0e94-d8d5-49e5-8152-d04f22e00db7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.L.P.S.® |
| Version Model Number | 110008333 |
| Catalog Number | 110008333 |
| 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 | 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 |
Customer Support Contacts
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868457869 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K132898
FDA Product Code
| HRS | Plate, fixation, bone |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
[00887868457869]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-11-30 |
| Device Publish Date | 2020-11-21 |
On-Brand Devices [A.L.P.S.®]
Trademark Results [A.L.P.S.]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 A.L.P.S. 86414170 not registered Dead/Abandoned |
Biomet C.V. 2014-10-03 |
 A.L.P.S. 86122580 4795950 Live/Registered |
Biomet C.V. 2013-11-19 |
 A.L.P.S. 85887976 not registered Dead/Abandoned |
Biomet C.V. 2013-03-27 |
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