← Back to catalogue

3-Ld Ecg Cable, Molded, Snap, A

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
3-LD ECG CABLE, MOLDED, SNAP, A FDA UDI
Generic Name
Electrocardiographic electrode connector FDA UDI
Device Name
3-LD ECG CABLE, MOLDED, SNAP, A FDA UDI
Model / Reference
CB-72307R FDA UDI
Description
3-LD ECG CABLE, MOLDED, SNAP, A FDA UDI

Identifiers

Catalog Number
5502 FDA UDI
Primary DI / UDI-DI
00840828145541 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
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

Category: Electrocardiographic electrode connector

3-Ld Ecg Cable, Molded, Snap, A by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode connector.

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 3d5d71ed-3aad-4da1-8352-f011709a156b 36 fields · synced May 30, 2026