Primary Device ID | 07290110640446 |
NIH Device Record Key | 9dadc1c6-af30-4bab-82d1-bf293868e146 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | T-Edge 10 |
Version Model Number | T-Edge 10 |
Catalog Number | AMS10-230-W-T |
Company DUNS | 600030209 |
Company Name | TUTTNAUER ISRAEL LTD. |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |