| Primary Device ID | 04026575418039 |
| NIH Device Record Key | d9056eda-28e0-41b7-90da-c616e48d5092 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LINK Instrument |
| Version Model Number | 319-400/04 |
| Catalog Number | 319-400/04 |
| Company DUNS | 315675488 |
| Company Name | WALDEMAR LINK GmbH & Co. KG |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 04026575418039 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
[04026575418039]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-05-08 |
| Device Publish Date | 2019-04-18 |