STERNALOCK® BLU SYSTEM 73-1302
GUDID 00888233011075
BIOMET MICROFIXATION, INC
Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | 00888233011075 |
| NIH Device Record Key | ca23b226-1328-4985-b8f3-3942cbae4b41 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STERNALOCK® BLU SYSTEM |
| Version Model Number | 73-1302 |
| Catalog Number | 73-1302 |
| Company DUNS | 046189866 |
| Company Name | BIOMET MICROFIXATION, INC |
| 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 | 00888233011075 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K111908
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
[00888233011075]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-07-08 |
| Device Publish Date | 2020-06-18 |
On-Brand Devices [STERNALOCK® BLU SYSTEM]
Trademark Results [STERNALOCK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STERNALOCK 78582263 3076302 Live/Registered |
ZIMMER BIOMET CMF AND THORACIC, LLC 2005-03-08 |
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