| Primary Device ID | 00880304628250 |
| NIH Device Record Key | 5b4152b4-0d46-4fb7-ab49-06d8e1552716 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | COMPREHENSIVE SHOULDER SYSTEM |
| Version Model Number | 41-405813 |
| Catalog Number | 41-405813 |
| 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 | true |
| 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 |
| 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 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304628250 [Primary] |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
[00880304628250]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-30 |
| Device Publish Date | 2016-10-25 |