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Anapod

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Anapod FDA UDI
Generic Name
Airway temperature monitoring system FDA UDI
Device Name
Anapod Humi-Therm Heated and Hunidified Anesthesia Heated Pediatric 96" Circuit FDA UDI
Model / Reference
A9246 FDA UDI
Description
Anapod Humi-Therm Heated and Hunidified Anesthesia Heated Pediatric 96" Circuit FDA UDI

Identifiers

Primary DI / UDI-DI
00709078007842 FDA UDI
510(k) Number
K904538 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Airway temperature monitoring system 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

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI f7e35a68-dc0e-4b5b-9afb-99597571eb8b 35 fields · synced May 31, 2026