Pulse Oximeter

GUDID 06934440102816

Shenzhen Viatom Technology Co., Ltd.

Pulse oximeter
Primary Device ID06934440102816
NIH Device Record Keyba950250-13d0-42b4-bd96-16c6f41c3341
Commercial Distribution StatusIn Commercial Distribution
Brand NamePulse Oximeter
Version Model NumberS10
Company DUNS421357243
Company NameShenzhen Viatom Technology Co., Ltd.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS106934440102816 [Primary]

FDA Product Code

OCHOximeter, Infrared, Sporting, Aviation

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-12-31
Device Publish Date2024-12-23

On-Brand Devices [Pulse Oximeter]

06934440102922S1
06934440102915SA-10BW
06934440102908S8-AW
06934440102892S6W
06934440102885S4
06934440102878S3
06934440102861S14
06934440102854S13B
06934440102847S13
06934440102830S12
06934440102823S11
06934440102816S10
06934440102809S9

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