FDA.reportPublic FDA data

MOBI

Primary DI
00891040702999
Brand
MOBI
Company
MOBI TECHNOLOGIES, INC.
Model
70299
Device description
MOBI’s Fingertip Pulse Oximeter offers a noninvasive method for monitoring oxygen salutation. Though its reading of peripheral oxygen saturation (SPO2). It is portable, lightweight and multi-functional that can perform the measurement within 10 seconds.
Published
2021-02-11
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true

Product Codes#

Code, Name table
CodeName
DQAOximeter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQAOximeterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K173123000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K173123000Pulse OximeterShenzhen Imdk Medical Technology Co., Ltd.2018-08-13DQA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10891040702996PackageGS16Not in Commercial Distribution
20891040702993PackageGS14Not in Commercial Distribution
00891040702999PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1089104070299610891040702996
2089104070299320891040702993
00891040702999008910407029998910407029990891040702999

GMDN Terms#

Term, Definition table
TermDefinition
Pulse oximeter, line-poweredA mains electricity (AC-powered) photoelectric device intended for the continuous transcutaneous measurement and display of haemoglobin oxygen saturation (SpO2). The signals, typically produced by light-emitting diodes (LEDs) and a receiving detector in a probe, or directly built-in, are used to make the measurements using the principle of spectrophotometry. The oximeter displays the SpO2 values and may calculate/display other parameters, e.g., pulse rate, electrocardiogram (ECG). The device is typically used bedside.

Regulatory Flags#

DUNS number
137468570
Device count
1
Lot or batch
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00891040701114MOBI701112020-05-07
00891040701138MOBI 701132020-04-08
00891040701169MOBI 701162020-03-25
10891040701166MOBI 701162020-03-25
00891040000279MOBI7000272022-07-31
00891040000309MOBI7000302022-07-31
00891040701008MOBI701002019-05-07
00891040000262MOBI7000262022-07-31
10891040000269MOBI7000262022-07-31
10891040000276MOBI7000272022-07-31
10891040000306MOBI7000302022-07-31
00891040701176MOBI701172022-03-28
10891040701173MOBI701172022-03-28
10891040702996MOBI702992021-02-11
00891040701190MOBI 701192017-08-30
00891040701671MOBI701672017-09-07
00891040702548MOBI702542017-09-07
00891040701251MOBI701252017-10-19
00891040701183MOBI 701182016-09-28
00891040701206MOBI 701202016-09-28

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00093351041099N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
00845717013550N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
00845717013567N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
06972040113849N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
06972040113856N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
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