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CoreTech RHB3003MN

by Vive Health LLC

CoreTech RHB3003MN is a sequential venous compression system (FDA Class II; FDA product code IRP, Massager, Powered Inflatable Tube) made by Vive Health LLC, listed in FDA GUDID since 23 Aug 2023 (UDI-DI 00810113573618), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810113573618 UDI-DI Date23 Aug 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  • Withdrawn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
CoreTech
Generic name
Sequential venous compression system
Model / reference
RHB3003MN
Primary DI / UDI-DI
00810113573618
FDA product code
IRP
GMDN term
Sequential venous compression system
Device class
Class II
Regulation number
890.5650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sequential venous compression system

Similar devices

Other devices filed under FDA product code IRP (Massager, Powered Inflatable Tube).

Other devices from Vive Health LLC

See all devices from Vive Health LLC →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)