CoreTech RHB3003M
CoreTech RHB3003M 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 19 May 2025 (UDI-DI 00810178880225), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810178880225 | Date19 May 2025 | StatusListed |
Official records
- AccessGUDID record 00810178880225
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CoreTech
- Generic name
- Sequential venous compression system
- Model / reference
- RHB3003M
- Primary DI / UDI-DI
- 00810178880225
- FDA product code
- IRP
- GMDN term
- Sequential venous compression system
- Device class
- Class II
- Regulation number
- 890.5650
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code IRP (Massager, Powered Inflatable Tube).
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- Powerpress Recovery Unit by HANURI DISTRIBUTION, INC
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- CERAGEM Master V6 CGM MB-1701 by Ceragem Co., Ltd.
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- Cold/Hot Compression by JKH Health Co., Ltd.
- Air Compression Leg Massager (UM605, UM606, UM607, UM608, UM609, UM610, UM611, UM617) by Shenzhen Urion Technology Co., Ltd
- INTERMITTENT COMPRESSION BOOT FOR OTC by Eischoco, Inc.