FDA.reportPublic FDA data

RENPHO Smart Blood Pressure Monitor

Primary DI
30860002249699
Brand
RENPHO Smart Blood Pressure Monitor
Company
JOICOM CORPORATION
Model
RP-BPM001S
Published
2020-09-15
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
DXNSystem, Measurement, Blood-Pressure, Non-Invasive

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DXNSystem, Measurement, Blood-Pressure, Non-InvasiveCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131395000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131395000TRANSTEK BLOOD PRESSURE MONITORGuangdong Transtek Medical Electronics Co., Ltd.2013-06-19DXN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
30860002249699PackageGS140In Commercial Distribution
00860002249698PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
3086000224969930860002249699
00860002249698008600022496988600022496980860002249698

GMDN Terms#

Term, Definition table
TermDefinition
Automatic-inflation electronic sphygmomanometer, portable, arm/wristAn electrically-powered device designed to noninvasively measure blood pressure using a self-contained software program that regulates automatic arm/wrist-cuff inflation and measurement cycles. It typically displays current heart rate and mean arterial pressure in addition to systolic and diastolic blood pressures; it may have memory to store blood pressure values and may sound an alarm if blood pressure exceeds pre-set limits. This device is designed to be portable (e.g., hand-held or carried in a pouch) and is often used for emergency services or home blood pressure monitoring.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
18444170149support@renpho.com

Regulatory Flags#

DUNS number
081060692
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
true
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
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00810140063168RENPHOR-MSC082026-08-18
00810140062833RENPHOPUS-R-WTR01-BK2026-07-24
00810140063113RENPHOPUS-R-WMV01-BU2026-07-24
00810140063120RENPHOPUS-R-WTR10-BK2026-07-24
00810140063106Renpho Massage GunR-WMG042026-07-21
00810140063052RenphoR-HAP092026-06-23
00810140063069RenphoR-HAP102026-06-23
00810140063076RenphoR-G0062026-06-23
00810140063083RenphoR-L0012026-06-23
00810140063090RenphoSKB-24182026-06-23
00810140063045RENPHO Eye MassagerR-WME062026-05-26
00810140063014RENPHOPUS-R-WMV01-2-BK2026-05-08
00810140063021RENPHOPUS-R-WMG18-BK2026-05-08
00810140063038RENPHOPUS-R-WMG09-GY2026-05-08
00810140063007RENPHOPUS-R-MSC05-BK2026-04-20
00810140062994RENPHOPUS-R-MSC06-BK2026-04-08

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00850078377302iHealthiHealth Labs Inc.DXN2026-10-12
00850078377326iHealthiHealth Labs Inc.DXN2026-10-12
06953825910501arboleafShenzhen Urion Technology Co., LtdDXN2026-10-10
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