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ResQPOD ITD 10

FDA UDI

Class II (US FDA UDI)

by Advanced Circulatory Systems Inc

Identity

Trade Name
ResQPOD ITD 10 FDA UDI
Generic Name
Cardiopulmonary resuscitation impedance valve, inspiratory FDA UDI
Device Name
The ResQPOD ITD 10 is indicated for the temporary increase in blood circulation. FDA UDI
Model / Reference
12-0242-000 FDA UDI
Description
The ResQPOD ITD 10 is indicated for the temporary increase in blood circulation. FDA UDI

Identifiers

Primary DI / UDI-DI
M5921202420000 FDA UDI
FDA Product Code
JOW FDA UDI
BWF FDA UDI
GMDN Term
Cardiopulmonary resuscitation impedance valve, inspiratory FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
868.5690 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

No

FDA UDI

Category: Cardiopulmonary resuscitation impedance valve, inspiratory

ResQPOD ITD 10 by Advanced Circulatory Systems Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary resuscitation impedance valve, inspiratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Circulatory Systems Inc

Sources (1)

  • FDA UDI a47e2f50-dd56-473d-be71-1fd2cafc16ca 33 fields · synced Jun 7, 2026