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Hmef

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
HMEF FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
HMEF Adult Inline Mini W/Sampling Port 150 - 1000 ML VT Range 26.77 ml Dead Space FDA UDI
Model / Reference
1002262 FDA UDI
Description
HMEF Adult Inline Mini W/Sampling Port 150 - 1000 ML VT Range 26.77 ml Dead Space FDA UDI

Identifiers

Primary DI / UDI-DI
00709078014246 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger/microbial medical gas filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heat/moisture exchanger/microbial medical gas filter

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

Similar devices

Also classified as Heat/moisture exchanger/microbial medical gas filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 1724c2a9-877c-46b0-bd9e-d03a013273f0 33 fields · synced May 31, 2026