1BYONE

Primary DI
10863696000337
Brand
1BYONE
Company
1BYONE PRODUCTS INC.
Model
JPD-500D
Device description
Pulse Oximeter
Published
2016-11-10
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

Product Codes#

Code, Name table
CodeName
DQAOximeter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQAOximeterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K140582000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K140582000FINGERTIP PULSE OXIMETERShenzhen Jumper Medical Equipment Co., Ltd.2014-08-28DQA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00863696000330PackageGS11In Commercial Distribution
10863696000337PackageGS1100In Commercial Distribution
00863696000323PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00863696000330008636960003308636960003300863696000330
1086369600033710863696000337
00863696000323008636960003238636960003230863696000323

GMDN Terms#

Term, Definition table
TermDefinition
Pulse oximeter, battery-poweredA portable, battery-powered, photoelectric device intended for the 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 applied to the fingertip or around the wrist; it may be used by healthcare facilities, emergency services, or in the home.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
845019202
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
108580690071291byonePL-029K16B2019-12-12
108580690070441BYONETMB-1585-BT2017-08-28
108636960003991BYONE725EU-00032017-05-24
108580690070201BYONE725EU-00022017-05-24
108636960003751BYONEPL-029K8(725EU-0001)2017-05-24
208580690070581byoneNT172018-04-12
108636960003511BYONEJPD-FR4012016-11-10

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