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Dar

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
DAR FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
Adult-Pediatric Mechanical Filter HME,Large FDA UDI
Model / Reference
354/5876 FDA UDI
Description
Adult-Pediatric Mechanical Filter HME,Large FDA UDI

Identifiers

Primary DI / UDI-DI
20884521056753 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

Yes

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

Category: Heat/moisture exchanger/microbial medical gas filter

Dar by Covidien LP — 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
Covidien LP

Sources (1)

  • FDA UDI 446d8413-9ad2-4b4e-b323-e681afc0662d 35 fields · synced Jun 8, 2026