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Hsiner

FDA UDI

Class II (US FDA UDI)

by Hsiner Company

Identity

Trade Name
Hsiner FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
HMEF REF70531 FDA UDI
Model / Reference
1 FDA UDI
Description
HMEF REF70531 FDA UDI

Identifiers

Catalog Number
70531 FDA UDI
Primary DI / UDI-DI
04712688057448 FDA UDI
510(k) Number
K091185 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Heat/moisture exchanger/microbial medical gas 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

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

Yes

FDA UDI

Category: Heat/moisture exchanger/microbial medical gas filter

Hsiner by Hsiner Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K091185 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hsiner Company

Sources (1)

  • FDA UDI e6490fe1-9764-4fee-9e5e-f4b30526cc5a 35 fields · synced Jun 7, 2026