Primary Device ID | 08809260470743 |
NIH Device Record Key | 21abf037-622d-4a2f-8bcd-5e5c640e9765 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRAUS ENDO |
Version Model Number | TRAUS ENDO #1 |
Company DUNS | 688019566 |
Company Name | Saeshin Precision Co., 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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809260470743 [Primary] |
EKX | Handpiece, Direct Drive, Ac-Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08809260470743]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-30 |
Device Publish Date | 2020-01-22 |
08809260470774 | '10:1 TRAUS MCE10XX+TRAUS XEW10+ACL(B)-46EP |
08809260470767 | '16:1 TRAUS MCE10XX+TRAUS XEW10+ACL(B)-42EP |
08809260470743 | 20:1 TRAUS MCE10XX+TRAUS XEW10+ACL(B)-41EP |
08809260470262 | Angle Handpiece |
08809260470255 | Angle Handpiece |
08809260470248 | Charger |
08809260470231 | Control Box |