Adult Circ w/ Insp HTD/W, Water Trap & AutoFCh

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name: Adult Circ w/ Insp HTD/W, Water Trap & AutoFCh FDA UDI
Generic Name: Ventilator breathing circuit, single-use FDA UDI
Model / Reference: 038-31-768U FDA UDI

Identifiers

Primary DI / UDI-DI: 05055788711957 FDA UDI
FDA Product Code: BTT FDA UDI
BZE FDA UDI
GMDN Term: Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5450 FDA UDI
868.5270 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Ventilator breathing circuit, single-use Heated respiratory humidifier

Adult Circ w/ Insp HTD/W, Water Trap & AutoFCh by Flexicare Medical Limited — 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: Flexicare Medical Limited

Sources (1)

FDA UDI a7b380e7-16fd-4571-a816-f0d7471fa9d1 32 fields · synced May 29, 2026