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Heated Circuit

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Heated Circuit FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
72` Ped.Htd Wick,BV,1LF,3pk ECG,GSL,14FR.O2 cath.,24` tube FDA UDI
Model / Reference
9313 FDA UDI
Description
72` Ped.Htd Wick,BV,1LF,3pk ECG,GSL,14FR.O2 cath.,24` tube FDA UDI

Identifiers

Primary DI / UDI-DI
00709078001086 FDA UDI
FDA Product Code
CAH FDA UDI
BZE FDA UDI
OFP FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
868.5270 FDA UDI
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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia breathing circuit, single-useHeat/moisture exchanger/microbial medical gas filterRespiratory gas heating wire, infant

Heated Circuit by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory gas heating wire, infant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 3bba506c-dbb6-42f6-aaa6-c74a063f9d0e 33 fields · synced May 30, 2026