Primary Device ID | 00860002308234 |
NIH Device Record Key | 34890ffa-f4a1-4c76-b01c-8fc7eff39029 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dr Trust |
Version Model Number | A310 |
Company DUNS | 081092844 |
Company Name | NURECA, INC. |
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 | false |
Lot Batch | true |
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 | 00860002308234 [Primary] |
OCH | Oximeter, Infrared, Sporting, Aviation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-16 |
Device Publish Date | 2020-07-08 |
00860002308203 | A310 |
08906101765676 | BP116A |
00860002308234 | A310 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DR TRUST 97272380 not registered Live/Pending |
Nureca Limited 2022-02-17 |
DR TRUST 90355616 not registered Live/Pending |
Nectar Biopharma 2020-12-02 |
DR TRUST 90355613 not registered Live/Pending |
Nectar Biopharma 2020-12-02 |