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ViveCare

FDA UDI

Class I (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
ViveCare FDA UDI
Generic Name
Cast/bandage waterproof bathing cover, single-use FDA UDI
Device Name
Waterproof Shower Protector (9x9") FDA UDI
Model / Reference
RHB3042CLR99CT7 FDA UDI
Description
Waterproof Shower Protector (9x9") FDA UDI

Identifiers

Primary DI / UDI-DI
00810113579245 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Cast/bandage waterproof bathing cover, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cast/bandage waterproof bathing cover, single-use

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

Similar devices

Also classified as Cast/bandage waterproof bathing cover, single-use.

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 878155c4-40da-4f99-ab62-17985b6e3733 33 fields · synced Jun 8, 2026