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ResScan

FDA UDI

Class II (US FDA UDI)

by Resmed Corp

Identity

Trade Name
ResScan FDA UDI
Generic Name
Ventilator application software FDA UDI
Device Name
RESSCAN V6.0.1 CD ASSY FDA UDI
Model / Reference
31334 FDA UDI
Description
RESSCAN V6.0.1 CD ASSY FDA UDI

Identifiers

Catalog Number
31334 FDA UDI
Primary DI / UDI-DI
00619498313341 FDA UDI
FDA Product Code
MNS FDA UDI
MNT FDA UDI
BZD FDA UDI
CBK FDA UDI
GMDN Term
Ventilator application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ventilator application software

ResScan by Resmed Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resmed Corp

Sources (1)

  • FDA UDI 28b903a6-ccf0-4ccc-8f43-9d641f151dd4 35 fields · synced Jun 8, 2026