Good Sense

Primary DI
10846036007692
Brand
Good Sense
Company
GEISS, DESTIN & DUNN, INC
Model
69-50C
Device description
GoodSense Pulse Oximeter
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQAOximeter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQAOximeterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K073454000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K073454000FINGERTIP PULSE OXIMETER, MODEL CMS-50CContec Medical System Co., Ltd.2008-05-05DQA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10846036007692PackageGS124In Commercial Distribution
30846036007696PackageGS13In Commercial Distribution
00846036007695PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1084603600769210846036007692
3084603600769630846036007696
00846036007695008460360076958460360076950846036007695

GMDN Terms#

Term, Definition table
TermDefinition
Pulse oximeter probe, reusableA photoelectric device applied externally to a body site, e.g., a fingertip, ear lobe, the bridge of nose, a toe, or the bridge of the foot of a paediatric or adult patient for the transcutaneous measurement of haemoglobin oxygen saturation (SpO2) in arterial blood using light detection. The signals, typically produced by light-emitting diodes (LEDs) and a receiving detector, are received by an oximeter to which this device is connected. The oximeter displays the SpO2 values and may calculate/display other parameters, e.g., electrocardiogram (ECG). This is a reusable device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-866-696-0957xx@xx.xx

Regulatory Flags#

DUNS number
076059836
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
00846036009453GOODSENSEG6009452025-01-16
00846036209457GOODSENSEG6009452025-01-16
00846036009446GOODSENSEG6009442022-05-03
00846036006438Good Sense69-3522016-09-23
00846036007671Good Sense69-3582016-09-23
00846036009774GOODSENSEG6009772025-01-16
00180410000880GoodSense1804100008802020-08-28
00180410000897GoodSense1804100008972020-08-28
00846036009606Good SenseKC009609MPSA1201GSGS2024-02-13
00846036006391Good Sense One Step Pregnancy TestFPPL2016-06-30
00846036009170Good SenseOne Step Pregnancy Test2020-09-21
00846036009187Good SenseOne Step Pregnancy Test2020-09-21
00846036006179Good Sense Early Result Pregnancy TestPLPL2016-06-30
00846036006186Good Sense Early Result Pregnancy TestPLPL2016-06-30
00846036006407Good Sense One Step Pregnancy TestFPPL2016-06-30
00846036002034Good SenseDS00203DS002032022-06-21
10846036002031Good SenseDS00203DS002032022-06-21
00846036000184Good Sense TamponsBGSAS202016-09-20
00846036000337Good Sense TamponsBGSAR082016-09-20
00846036003161Good Sense TamponsBGSGR202016-09-20

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