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TrueCPR™ Coaching Device

FDA UDI

Class II (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
TrueCPR™ Coaching Device FDA UDI
Generic Name
Cardiopulmonary resuscitation feedback device, electronic FDA UDI
Device Name
TRUECPR,PACKAGED,MULTI-LANGUAGE, CONFIG B FDA UDI
Model / Reference
80596 FDA UDI
Description
TRUECPR,PACKAGED,MULTI-LANGUAGE, CONFIG B FDA UDI

Identifiers

Catalog Number
80596-000003 FDA UDI
Primary DI / UDI-DI
00883873890455 FDA UDI
FDA Product Code
LIX FDA UDI
GMDN Term
Cardiopulmonary resuscitation feedback device, electronic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5210 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cardiopulmonary resuscitation feedback device, electronic

TrueCPR™ Coaching Device by PHYSIO-CONTROL, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary resuscitation feedback device, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI abd7e219-fcc4-44dc-9b0d-3eebdecc9c93 35 fields · synced Jun 9, 2026