Fitfaith

GUDID 06970953261107

Shenzhen Fitfaith Technology Co., Ltd

Pulse oximeter, battery-powered
Primary Device ID06970953261107
NIH Device Record Keybfb1c1e0-71ff-4ed1-87d4-d4eaa313e912
Commercial Distribution Discontinuation2020-12-31
Commercial Distribution StatusIn Commercial Distribution
Brand NameFitfaith
Version Model NumberM110
Company DUNS544436982
Company NameShenzhen Fitfaith Technology Co., Ltd
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106970953261107 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQAOximeter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-08-30
Device Publish Date2018-05-15

On-Brand Devices [Fitfaith]

06970953261305M130
06970953261107M110
06970953260094M160E
06970953260087M230E
06970953260070M170E
06970953260063M130E
06970953260056M110E
06970953260049M230
06970953260032M170
06970953260025M160

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