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QUIK-COMBO Therapy cable to FAST-PATCH® Adapter Cable

FDA UDI

Class III (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
QUIK-COMBO Therapy cable to FAST-PATCH® Adapter Cable FDA UDI
Generic Name
External defibrillation electrode, adult, reusable FDA UDI
Device Name
CABLE ASSY - FAST-PATCH,DOMESTIC FDA UDI
Model / Reference
11110 FDA UDI
Description
CABLE ASSY - FAST-PATCH,DOMESTIC FDA UDI

Identifiers

Catalog Number
11110-000052 FDA UDI
Primary DI / UDI-DI
00681490583398 FDA UDI
FDA Product Code
MKJ FDA UDI
GMDN Term
External defibrillation electrode, adult, reusable FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.5310 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: External defibrillation electrode, adult, reusable

QUIK-COMBO Therapy cable to FAST-PATCH® Adapter Cable by PHYSIO-CONTROL, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External defibrillation electrode, adult, reusable.

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 c0992b4a-0d7c-4fa6-a42b-9b5353b1dc31 35 fields · synced Jun 9, 2026