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LW MULTI-LINK, 5LEAD, Slw, PINCH, 29", GR

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
LW MULTI-LINK,5LEAD,Slw,PINCH,29",GR FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
LW MULTI-LINK,5LEAD,Slw,PINCH,29",GR FDA UDI
Model / Reference
LDW-05BD-29GR-0000 FDA UDI
Description
LW MULTI-LINK,5LEAD,Slw,PINCH,29",GR FDA UDI

Identifiers

Catalog Number
9001 FDA UDI
Primary DI / UDI-DI
00840828130592 FDA UDI
510(k) Number
K081762 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
Not 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

LW MULTI-LINK, 5LEAD, Slw, PINCH, 29", GR by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2fa9ab61-f4f3-4b77-8781-726735a470ad 37 fields · synced May 31, 2026