| Primary Device ID | 00887868545504 |
| NIH Device Record Key | b0eaed37-8a84-4c4b-b866-1716074a966f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CANCELLOUS LAG SCREW |
| Version Model Number | 8155-40-030 |
| Catalog Number | 815540030 |
| 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 | 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 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868545504 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
[00887868545504]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-15 |
| Device Publish Date | 2022-09-07 |