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Vive

FDA UDI

Class II (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
Vive FDA UDI
Generic Name
Portable sequential venous compression system FDA UDI
Device Name
Arm Compression Pump (Full System) Premium FDA UDI
Model / Reference
RHB2098BLK FDA UDI
Description
Arm Compression Pump (Full System) Premium FDA UDI

Identifiers

Primary DI / UDI-DI
00810113570716 FDA UDI
510(k) Number
K192358 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Portable sequential venous compression system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Portable sequential venous compression system

Vive by Vive Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable sequential venous compression system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vive Health Llc

Sources (1)

  • FDA UDI fe275e49-c9fd-4b17-a264-da3fd88f914b 34 fields · synced Jun 6, 2026