Primary Device ID | 03760177042742 |
NIH Device Record Key | 6de34948-4480-40d0-95c5-9b1858e9a3e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Euroscrew NG |
Version Model Number | Ø8 L30 |
Catalog Number | T720830NG |
Company DUNS | 764746723 |
Company Name | TEKNIMED |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |