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Roscoe

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
ROSCOE FDA UDI
Generic Name
Ultraviolet device disinfection chamber FDA UDI
Device Name
ULTRA-5 ULTRAVIOLET DISINFECTOR (UV-C) - CPAP, CPAP ACCESSORIES, MULTIPURPOSE SANITIZER FDA UDI
Model / Reference
ULTRA-5 FDA UDI
Description
ULTRA-5 ULTRAVIOLET DISINFECTOR (UV-C) - CPAP, CPAP ACCESSORIES, MULTIPURPOSE SANITIZER FDA UDI

Identifiers

Primary DI / UDI-DI
00092237623862 FDA UDI
FDA Product Code
MEC FDA UDI
GMDN Term
Ultraviolet device disinfection chamber FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6992 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Roscoe by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f242df84-2ad0-4354-9e82-3f5e364f1c08 35 fields · synced May 31, 2026