| Primary Device ID | 00888233056953 |
| NIH Device Record Key | b35d3abe-79ea-4e99-a7d4-3de50199d393 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PECTUS SYSTEM |
| Version Model Number | PS-2024 |
| 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 | true |
| 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 | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM | |
| Phone | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM | |
| Phone | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM | |
| Phone | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM | |
| Phone | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM | |
| Phone | 904-741-4400 |
| FXJAX-ORDERS@BIOMET.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888233056953 [Primary] |
| HRS | Plate, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888233056953]
Moist Heat or Steam Sterilization
[00888233056953]
Moist Heat or Steam Sterilization
[00888233056953]
Moist Heat or Steam Sterilization
[00888233056953]
Moist Heat or Steam Sterilization
[00888233056953]
Moist Heat or Steam Sterilization
[00888233056953]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-27 |
| Device Publish Date | 2022-05-19 |