← Back to catalogue

Patient Leadwire

FDA UDI

Class II (US FDA UDI)

by Merit Cables Incorporated

Identity

Trade Name
Patient Leadwire FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Leadwire Adapter 3mm Socket to Termination, Various Lengths & Colors FDA UDI
Model / Reference
20100-3mm-X FDA UDI
Description
Leadwire Adapter 3mm Socket to Termination, Various Lengths & Colors FDA UDI

Identifiers

Primary DI / UDI-DI
90817266020184 FDA UDI
510(k) Number
K942321 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic lead set, reusable 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 120 Inch FDA UDI
Length — 60 Inch FDA UDI
Length — 40 Inch FDA UDI
Length — 24 Inch FDA UDI
Length — 18 Inch FDA UDI
Length — 14 Inch FDA UDI

Category: Electrocardiographic lead set, reusable

Patient Leadwire by Merit Cables Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 59d3b0e0-68bb-44c7-8ef3-a1d10c6f75ea 36 fields · synced Jun 8, 2026