Breathing Circuit

FDA UDI

Class II (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name: Breathing Circuit FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: Sunset Pediatric Active Circuit with Water Trap, Non-heated, Respironics #1073220 & #1073229 FDA UDI
Model / Reference: VC1001P FDA UDI
Description: Sunset Pediatric Active Circuit with Water Trap, Non-heated, Respironics #1073220 & #1073229 FDA UDI

Identifiers

Primary DI / UDI-DI: 00848530091606 FDA UDI
FDA Product Code: CAH FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5260 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Breathing Circuit by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: SUNSET HEALTHCARE SOLUTIONS, Inc.

Sources (1)

FDA UDI d6b69c08-d0a8-44d6-8f36-59842ab7fe3b 34 fields · synced May 31, 2026