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 Passive Circuit with Water Trap, Non-heated, Respironics #1073224 & #1073233 FDA UDI
Model / Reference: VC1004P FDA UDI
Description: Sunset Pediatric Passive Circuit with Water Trap, Non-heated, Respironics #1073224 & #1073233 FDA UDI

Identifiers

Primary DI / UDI-DI: 00848530091590 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 34c043bf-ea9e-4d83-9199-2cabacf15024 34 fields · synced Jun 1, 2026