Primary Device ID | 04026575157679 |
NIH Device Record Key | 352931c4-78b1-4e1e-9ed5-e6a0af080f70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LINK Instruments - Fixation instruments |
Version Model Number | 319-560/02 |
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 |
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