Skintact

FDA UDI

Class II (US FDA UDI)

by Leonhard Lang Co.

Identity

Trade Name: SKINTACT FDA UDI
Generic Name: Neonatal electrocardiographic electrode FDA UDI
Device Name: Pre-wired ECG Electrode FDA UDI
Model / Reference: PD50-F4C FDA UDI
Description: Pre-wired ECG Electrode FDA UDI

Identifiers

Catalog Number: PD50-F4C FDA UDI
Primary DI / UDI-DI: 19005531000435 FDA UDI
FDA Product Code: DRX FDA UDI
GMDN Term: Neonatal electrocardiographic electrode 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Neonatal electrocardiographic electrode

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Leonhard Lang Co.

Sources (1)

FDA UDI 773338c0-fc54-4d8f-a1d0-ea6c4602e1e5 35 fields · synced Jun 1, 2026