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Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit FDA UDI
Generic Name
Respiratory gas heating wire, adult FDA UDI
Device Name
Adult Heated Humidified Circuit, expandable up to 96" FDA UDI
Model / Reference
A9241 FDA UDI
Description
Adult Heated Humidified Circuit, expandable up to 96" FDA UDI

Identifiers

Primary DI / UDI-DI
00709078004490 FDA UDI
510(k) Number
K904538 FDA UDI
FDA Product Code
BZE FDA UDI
GMDN Term
Respiratory gas heating wire, adult FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5270 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Anapod™ Humi-therm Heated and Humidified Wick Breathing Circuit by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K904538 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 89940c60-7ea8-4f53-aeca-ddbb0a4f66f7 35 fields · synced Jun 8, 2026