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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
Respiratory gas heating wire, adult FDA UDI
Device Name
60` 28V Adult Htd Limb, St Water, 40 CM Pop Off Valve, 15` FDA UDI
Model / Reference
9411 FDA UDI
Description
60` 28V Adult Htd Limb, St Water, 40 CM Pop Off Valve, 15` FDA UDI

Identifiers

Primary DI / UDI-DI
00709078001154 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Respiratory gas heating wire, adult FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 8c7df8c2-1404-49b2-9c72-1f20bb0012dc 34 fields · synced May 30, 2026