← Back to catalogue

Quik-Combo Therapy Cable

FDA UDI

Class III (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
Quik-Combo Therapy Cable FDA UDI
Generic Name
External defibrillation electrode, adult, reusable FDA UDI
Device Name
CABLE-THERAPY, QUIK-COMBO, SUPPLIED ASSY, ROHS FDA UDI
Model / Reference
11113 FDA UDI
Description
CABLE-THERAPY, QUIK-COMBO, SUPPLIED ASSY, ROHS FDA UDI

Identifiers

Catalog Number
11113-000004 FDA UDI
Primary DI / UDI-DI
00883873990650 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 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI 0f5d6f57-93d8-486f-8e9b-8b2b3ebd4713 35 fields · synced Jun 9, 2026