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Ventiflow Circuit 108" With CO2 Monitoring Line 2L Reservoir Bag B/V Filter And

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Ventiflow Circuit 108" With CO2 Monitoring Line 2L Reservoir Bag B/V Filter And FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Model / Reference
038-01-862U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788775027 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

Yes

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 Circuit 108" With CO2 Monitoring Line 2L Reservoir Bag B/V Filter And 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 6597763a-3702-4ff9-a712-23a358b664e3 32 fields · synced Jun 1, 2026