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S8

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
S8 FDA UDI
Generic Name
Heat/moisture exchanger insertable filter FDA UDI
Device Name
S8/TYPE A HYPO FILTERS FDA UDI
Model / Reference
33919 FDA UDI
Description
S8/TYPE A HYPO FILTERS FDA UDI

Identifiers

Catalog Number
33919 FDA UDI
Primary DI / UDI-DI
00619498339198 FDA UDI
510(k) Number
K071171 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Heat/moisture exchanger insertable filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heat/moisture exchanger insertable filter

S8 by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger insertable filter.

Cleared under the same submission

K071171 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resmed Pty Ltd

Sources (1)

  • FDA UDI a5281579-2aa4-414b-88bc-44b6496298c4 37 fields · synced May 30, 2026