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Cbl 024, Twin, 5ld, Yoke, 25ft, Aha, Intermed

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
CBL 024,TWIN,5LD,YOKE,25FT,AHA,INTERMED FDA UDI
Generic Name
Electrocardiographic electrode connector FDA UDI
Device Name
CBL 024,TWIN,5LD,YOKE,25FT,AHA,INTERMED FDA UDI
Model / Reference
CBT-05JB-10CS-3121 FDA UDI
Description
CBL 024,TWIN,5LD,YOKE,25FT,AHA,INTERMED FDA UDI

Identifiers

Catalog Number
18668 FDA UDI
Primary DI / UDI-DI
00840828139779 FDA UDI
510(k) Number
K081762 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode connector 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

Cbl 024, Twin, 5ld, Yoke, 25ft, Aha, Intermed 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 3e3e9b9c-1670-4ec5-8ec1-a5e17879a660 37 fields · synced May 31, 2026