| Primary Device ID | 07640181161492 |
| NIH Device Record Key | 13df5c8d-296b-4390-bd79-837bed252079 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pattern PIP 3 |
| Version Model Number | 211-A20003 |
| Company DUNS | 480138827 |
| Company Name | Keri Medical SA |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640181161492 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
[07640181161492]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-30 |
| Device Publish Date | 2022-11-22 |