Primary Device ID | 04026575018475 |
NIH Device Record Key | dcd08ca3-2b07-4905-b8de-674e36b7aa14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boneplate |
Version Model Number | 10-5367/02 |
Catalog Number | 10-5367/02 |
Company DUNS | 315675488 |
Company Name | WALDEMAR LINK GmbH & Co. KG |
Device Count | 1 |
DM Exempt | true |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |