FDA.reportPublic FDA data

MOBI

Primary DI
10891040702996
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
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

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
10891040702996PackageGS16In Commercial Distribution
20891040702993PackageGS14In 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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
137468570
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00891040701114MOBI701112020-05-07
00891040701138MOBI 701132020-04-08
00891040701169MOBI 701162020-03-25
00891040702999MOBI702992021-02-11
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
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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00010939962218N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
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
06931973400563CaremedShenzhen Caremed Medical Technology Co., Ltd.DQA2026-07-09
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