Flexicare

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name: Flexicare FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: Adult Exp Circuit 96” L/Y-Piece Plain Elbow 2xBV + 1xHMEF Filter Size 5 Mask & 3LRes Bag 10ft.M/Line FDA UDI
Model / Reference: 038-01-845BU FDA UDI
Description: Adult Exp Circuit 96” L/Y-Piece Plain Elbow 2xBV + 1xHMEF Filter Size 5 Mask & 3LRes Bag 10ft.M/Line FDA UDI

Identifiers

Primary DI / UDI-DI: 05055931103097 FDA UDI
FDA Product Code: CAI FDA UDI
CCK FDA UDI
CAH FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5240 FDA UDI
868.1400 FDA UDI
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

Yes

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: Anaesthesia breathing circuit, single-use

Flexicare by Flexicare Medical Limited — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Flexicare Medical Limited

Sources (1)

FDA UDI 13e94363-9774-4fa2-a713-08bf70df8281 33 fields · synced May 30, 2026