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Lead Wire, Snap To Nihon Konden

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
LEAD WIRE, SNAP TO NIHON KONDEN FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
LEAD WIRE, SNAP TO NIHON KONDEN FDA UDI
Model / Reference
DLW-06AF-MXAN-0000 FDA UDI
Description
LEAD WIRE, SNAP TO NIHON KONDEN FDA UDI

Identifiers

Catalog Number
19778 FDA UDI
Primary DI / UDI-DI
90840828101526 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic electrode, single-use

Lead Wire, Snap To Nihon Konden by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Curbell Medical Products, Inc.

Sources (1)

  • FDA UDI d6bbe37e-d1b1-4227-b6f0-f6b173a3731f 35 fields · synced Jun 1, 2026