| Primary Device ID | 04026575082056 |
| NIH Device Record Key | 92af99ec-73ef-44cc-afd1-1bd4452f0127 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MP Reconstruction System - Instruments |
| Version Model Number | 134-202/00 |
| Company DUNS | 315675488 |
| Company Name | WALDEMAR LINK GmbH & Co. KG |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04026575082056 [Primary] |
| FZX | Guide, surgical, instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
[04026575082056]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-05-03 |
| Device Publish Date | 2022-12-20 |
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