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Carex

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Carex FDA UDI
Generic Name
Non-respiratory device ambient air filter FDA UDI
Device Name
EQ DRMST FILTER REUS FDA UDI
Model / Reference
FGC155EQ WMRT FDA UDI
Description
EQ DRMST FILTER REUS FDA UDI

Identifiers

Primary DI / UDI-DI
00681131116350 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Non-respiratory device ambient air filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-respiratory device ambient air filter

Carex by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-respiratory device ambient air filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bd8fda3-3ce5-49f7-a23c-272b81629175 34 fields · synced May 31, 2026