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Skintact

FDA UDI

Class II (US FDA UDI)

by Leonhard Lang Co.

Identity

Trade Name
Skintact FDA UDI
Generic Name
Electrocardiographic electrode connector FDA UDI
Device Name
Accessory for ECG Electrodes FDA UDI
Model / Reference
EASICLIP FDA UDI
Description
Accessory for ECG Electrodes FDA UDI

Identifiers

Catalog Number
EASICLIP FDA UDI
Primary DI / UDI-DI
19005531000107 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic electrode connector

Skintact by Leonhard Lang Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Leonhard Lang Co.

Sources (1)

  • FDA UDI 07d749bc-2746-4c8c-8ada-6c87ced79fbc 34 fields · synced May 29, 2026