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TeleRPM

FDA UDI

Class II (US FDA UDI)

by Guangdong Transtek Medical Electronics Co., Ltd

Identity

Trade Name
TeleRPM FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
Pro Cellular Blood Pressure Monitor FDA UDI
Model / Reference
LS802-GP FDA UDI
Description
Pro Cellular Blood Pressure Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
06932825301595 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

TeleRPM by Guangdong Transtek Medical Electronics Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, portable, arm/wrist.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81dd851a-28b0-4acf-8efb-43fc334dcd90 33 fields · synced Jun 8, 2026