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TeleRPM GBF-2008-B

by Guangdong Transtek Medical Electronics Co., Ltd

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 Number06932825306118 UDI-DI Date29 May 2026ListedStatusListed 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  • Withdrawn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
Bioelectrical body composition analyser
Model / Reference
GBF-2008-B
Primary DI / UDI-DI
06932825306118
FDA Product Code
PUH
GMDN Term
Bioelectrical body composition analyser
Device Class
Class II
Regulation Number
870.2770
GUDID distribution status
In Commercial Distribution

Other devices from Guangdong Transtek Medical Electronics Co., Ltd

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Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

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