MOBI

Primary DI
10891040000269
Brand
MOBI
Company
MOBI TECHNOLOGIES, INC.
Model
700026
Device description
Smart DualScan Ear + Forehead Bluetooth Thermometer
Published
2022-07-31
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
FLLThermometer, Electronic, Clinical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FLLContinuous Measurement ThermometerGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K172795000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K172795000Infrared ThermometerShenzhen Jumper Medical Equipment Co., Ltd.2018-03-14FLL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10891040000269PackageGS13In Commercial Distribution
20891040000266PackageGS112In Commercial Distribution
00891040000262PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1089104000026910891040000269
2089104000026620891040000266
00891040000262008910400002628910400002620891040000262

GMDN Terms#

Term, Definition table
TermDefinition
Infrared patient thermometer, ear/skinA hand-held, battery-powered, electronic instrument designed to measure: 1) the temperature of a patient's ear canal, typically to estimate the internal (core) temperature; and 2) the temperature of a site on the skin (e.g., axilla, forehead), by measurement of body infrared emissions. It typically includes both a skin-surface tip and an intra-aural tip. This device is intended for use in the home or healthcare facility. This is a reusable device.

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
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

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Primary DI, Brand, Company table
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00850086928022SENSINEL™ CARDIOPULMONARY MANAGEMENT (CPM) SYSTEM)Analog Devices, Inc.FLL2026-06-03
00850086928039SENSINEL™ CARDIOPULMONARY MANAGEMENT (CPM) SYSTEM)Analog Devices, Inc.FLL2026-06-03
08720256776567Corsano CardioWatch 287-2 SystemCorsano Health B.V.FLL2026-06-02
06926347900459joybabeShenzhen Brav Electronic Technologies Co., Ltd.FLL2026-06-01
06942284618073One Step®JOYTECH HEALTHCARE CO.,LTDFLL2026-05-29
00884392020613Safety 1stDOREL JUVENILE GROUP, INC.FLL2026-05-28
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08698870325211FMTMETKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETIFLL2026-04-22