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Bed Buddy TPF201RB

by Drive Devilbiss Healthcare

Bed Buddy TPF201RB is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 2 May 2023 (UDI-DI 00749836002016), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00749836002016 UDI-DI Date2 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Bed Buddy
Generic name
Moist-heat pack
Model / reference
TPF201RB
Primary DI / UDI-DI
00749836002016
FDA product code
IME
GMDN term
Moist-heat pack
Device class
Class I
Regulation number
890.5700
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IME (Pack, Hot Or Cold, Reusable).

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)