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S9

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
S9 FDA UDI
Generic Name
Portable electric ventilator FDA UDI
Device Name
DC/DC CONVERTER - 24V/90W FDA UDI
Model / Reference
36970 FDA UDI
Description
DC/DC CONVERTER - 24V/90W FDA UDI

Identifiers

Catalog Number
36970 FDA UDI
Primary DI / UDI-DI
00619498369706 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Portable electric ventilator 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable electric ventilator

S9 by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable electric ventilator.

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 86d822c0-c488-40da-9345-936971e03c55 35 fields · synced May 30, 2026