| Primary Device ID | 00880304565982 |
| NIH Device Record Key | ca6c01b3-f33a-4bc8-9c98-86924c1ad4e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G7 PROVISIONAL HIGH WALL LINER |
| Version Model Number | 010002666 |
| Catalog Number | 010002666 |
| 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 |
| 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 | 00880304565982 [Primary] |
| PBI | prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
[00880304565982]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-09-23 |
| 00880304566033 | 010002678 |
| 00880304566026 | 010002676 |
| 00880304566019 | 010002675 |
| 00880304566002 | 010002670 |
| 00880304565999 | 010002667 |
| 00880304565982 | 010002666 |
| 00880304565975 | 010002665 |
| 00880304565968 | 010002664 |
| 00880304565951 | 010002663 |
| 00880304565944 | 010002660 |
| 00880304565937 | 010002659 |
| 00880304565920 | 010002658 |
| 00880304565913 | 010002657 |
| 00880304565906 | 010002656 |
| 00880304565883 | 010002653 |
| 00880304565876 | 010002652 |
| 00880304565869 | 010002651 |
| 00880304565852 | 010002650 |
| 00880304565845 | 010002649 |
| 00880304565838 | 010002648 |
| 00880304565821 | 010002647 |
| 00880304553866 | 010002677 |
| 00880304551862 | 010002655 |
| 00880304551855 | 010002645 |
| 00880304551848 | 010002646 |
| 00880304551770 | 010002674 |
| 00880304551763 | 010002673 |
| 00880304551640 | 010002672 |
| 00880304551633 | 010002671 |
| 00880304551480 | 010002668 |
| 00880304551459 | 010002669 |
| 00880304551343 | 010002662 |
| 00880304551282 | 010002661 |