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Leadwire Wht 24"dn/Sn

FDA UDI

Class II (US FDA UDI)

by Rpi

Identity

Trade Name
LEADWIRE WHT 24"DN/SN FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Model / Reference
LSW002 FDA UDI

Identifiers

Catalog Number
LSW002 FDA UDI
Primary DI / UDI-DI
00841034114727 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

No

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

Category: Electrocardiographic lead set, reusable

Leadwire Wht 24"dn/Sn by Rpi — 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

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Manufacturer

Manufacturer
Rpi

Sources (1)

  • FDA UDI f9dd6534-2cd1-4b66-8ec7-9e35709e4a3e 35 fields · synced May 30, 2026