Primary Device ID | 07290110640132 |
NIH Device Record Key | 806565fc-2b05-4a78-b9dd-2828e0458c49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EZ10 |
Version Model Number | EZ10 |
Catalog Number | TTA-EZ10-115V-P |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290110640132 [Primary] |
FLE | Sterilizer, Steam |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-17 |
Device Publish Date | 2018-09-16 |
07290110640132 | Sterilizer,steam |
07290110640125 | Sterilizer,steam |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EZ10 76585102 2983757 Live/Registered |
TUTTNAUER USA CO. LTD. 2004-04-05 |