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TeleRPM TMB-2092-G

by Guangdong Transtek Medical Electronics Co., Ltd 3 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06932825303278 UDI-DI Date10 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
TeleRPM
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / Reference
TMB-2092-G
Primary DI / UDI-DI
06932825303278
FDA Product Code
DXN
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Guangdong Transtek Medical Electronics Co., Ltd

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Properties

  • Single Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No