A.L.P.S.® CLAVICLE PLATING SYSTEMCLAVICLE DEPTH GAUGE 233500003
GUDID 00880304834613
Biomet Orthopedics, LLC
Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable| Primary Device ID | 00880304834613 |
| NIH Device Record Key | e89fd4d0-2452-4a7a-bd16-4291b9454818 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.L.P.S.® CLAVICLE PLATING SYSTEMCLAVICLE DEPTH GAUGE |
| Version Model Number | 233500003 |
| Catalog Number | 233500003 |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304834613 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K173767
FDA Product Code
| HRS | Plate, fixation, bone |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
[00880304834613]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2019-02-08 |
Devices Manufactured by Biomet Orthopedics, LLC
| 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 |
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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