Skintact

Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring

Registry build 21.09.26
3manufacturers in China registered for this device type
11catalogue numbers in this listing
5510(k) clearances naming this product code
5recalls on this code

Who Else Makes It

All of them in Guangdong. 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MKJ
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9

Record

Regulatory record for Skintact
Listed by Leonhard Lang Gmbh, Austria
FDA product code MKJ
Device type Automated External Defibrillators (Non-Wearable)
Device class Class 3
Regulation 21 CFR 870.5310
Establishment Contract manufacturer, Manufacturer
Record published 2015-03-20
Record revised 2025-08-18 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Storage environment temperature 0 to 50 °C
Packaging Box of 10, box of 6, case of 6
Distribution end date 2015-06-17

Catalogue Numbers

Catalogue numbers for Skintact
Catalogue number Size Status
DF59NC In distribution
DF20N In distribution
DF27NC In distribution
DF29N In distribution
DF28NC In distribution
DF27N In distribution
DF59N In distribution
DF20NC In distribution
DF28N In distribution
DF26N In distribution
DF82I Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
X Series Zoll Medical Corporation 862
E Series Zoll Medical Corporation 571
M Series Zoll Medical Corporation 219
R Series Zoll Medical Corporation 216
Lifepak® 15 monitor/defibrillator Physio-Control, Inc. 188
AED Plus Zoll Medical Corporation 124
Lifepak® 12 defibrillator/monitor Physio-Control, Inc. 122
Lifepak CR Plus and Lifepak Express defibrillators Physio-Control, Inc. 111
M Series Biphasic Zoll Medical Corporation 111
PadPro ConMed Corporation 96
R&D Batteries, Inc. R & D Batteries, Inc. 71
Lifepak® 20 and Lifepak 20e defibrillator/monitors Physio-Control, Inc. 59

Showing 12 of 312. All products under Automated External Defibrillators (Non-Wearable)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K142803 2014-12-02
K103186 2011-02-08
K081371 2008-09-24
K072233 2007-10-05
K041883 2004-09-07

Recalls

3 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2017-08-08 Class I Component design/selection Certain lots of the defibrillation electrodes model DF59N and DF59NC may have a delay in connecting or not connect at all with the defibrillator ZOLL AED PLUS. This may cause a situation in which a patient, who is in a life threatening cond 8,249 units total 2020-06-09
2016-09-01 Class I Device Design There is a risk that defibrillation electrodes model DF29N will be connected with the defibrillator Welch Allyn AED 10 only with delay or not at all. This may cause a situation in which a patient, who is in a life threatening condition and 11,110 ( US 8,040; OUS 3,070) 2019-03-26
2014-12-03 Class I Component design/selection The firm discovered that during the use of these defibrillation electrodes a possibility for arcing and a resulting malfunction exists. This could lead to a situation, in which a patient who is in a life threatening situation requiring a d 1080 pieces 2015-08-13
2009-07-10 Not classified Nonconforming Material/Component A potential risk was identified associated with the connectors of the defibrillation electrodes DF20. It was found that some of the connectors do not slip easily into the sockets of the defibrillator or an extension cord of the defibrillato 1433 USA 2011-12-17
2009-07-10 Not classified Nonconforming Material/Component A potential risk was identified associated with the connectors of the defibrillation electrodes DF20. It was found that some of the connectors do not slip easily into the sockets of the defibrillator or an extension cord of the defibrillato 3044 2011-12-17

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P160008 2026-05-07 HeartSine’s samaritan® Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P) and Accessories Heartsine Technologies, Ltd
P170018 2025-11-06 LIFEPAK® CR2 Automated External Defibrillator Physio-Control, Inc.
P160032 2025-07-03 Defibtech Lifeline; Defibtech Lifeline AUTO; Defibtech Lifeline VIEW; Defibtech Lifeline VIEW AUTO; Defibtech Lifeline E Defibtech, LLC
P210015 2025-01-29 Avive Automated External Defibrillator (AED) System Avive Solutions Inc
P200005 2024-01-09 TZ Medical Defibrillation Electrodes, Accessory Cables, and Connectors TZ Medical, Inc.
P200007 2023-06-23 HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads Graphic Controls D.B.A. Vermed
P200004 2022-06-16 ConMed PadPro Multifunction Electrodes ConMed Corporation
P160012 2021-07-08 Infant/Child Reduced Energy Defibrillation Electrodes Physio-Control, Inc.
P160033 2021-06-14 Powerheart G5 AED Zoll Medical Corporation
P190013 2021-02-02 AED Battery Exchange (Models 9146-ABE, G5-ABE, 5070-ABE, FR3-ABE) AED Battery Exchange, LLC
P180028 2020-08-22 HeartStart FRx Defibrillator Philips Medical Systems Technologies Ltd
P190007 2020-08-07 Cardinal Health Multifunctional Defibrillation Electrode Cardinalhealth
P160022 2020-06-11 X Series and Propaq MD Zoll Medical Corporation
P160015 2020-06-05 AED 3 Defibrillator with Uni-Padz Zoll Medical Corporation
P160028 2020-05-11 Philips HeartStart FR3 Defibrillator Philips Medical Systems Technologies Ltd
P160026 2020-02-13 LIFEPAK Automated External Defibrillators (AEDs) Physio-Control, Inc.
P160034 2019-08-20 Powerheart® G3 Pro AED Zoll Medical Corporation

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer