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Ventiflow Basic Coaxial Circuit 72" Luer Elbow 2 x B/V Filter 1 HMEF 3L Res Bag

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Ventiflow Basic Coaxial Circuit 72" Luer Elbow 2 x B/V Filter 1 HMEF 3L Res Bag FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Model / Reference
038-01-754U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788747543 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Ventiflow Basic Coaxial Circuit 72" Luer Elbow 2 x B/V Filter 1 HMEF 3L Res Bag by Flexicare Medical Limited — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9cb7b356-d585-45cf-bdcd-7adbe980759e 32 fields · synced Jun 8, 2026