Primary Device ID | 00628693098014 |
NIH Device Record Key | df850668-142e-44e8-900c-64072aea20c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ByFloProducts |
Version Model Number | PG-IRT1602 |
Company DUNS | 208296406 |
Company Name | Byflo Products Inc. |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00628693098014 [Primary] |
GS1 | 10628693098011 [Package] Package: Box [60 Units] In Commercial Distribution |
FLL | Thermometer, Electronic, Clinical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-17 |
Device Publish Date | 2022-02-09 |
00628693098014 | Infrared Forehead Thermometer |
10628693098035 | Non-contact Infrared Thermometer |
10628693098042 | Pulse Oximeter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BYFLOPRODUCTS 97416872 not registered Live/Pending |
Ogier, Florimond 2022-05-18 |