← Back to catalogue

Cadwell Shielded Cable

FDA UDI

Class II (US FDA UDI)

by Cadwell Industries, Inc.

Identity

Trade Name
Cadwell Shielded Cable FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Device Name
Cable, Reusable Shielded Mono with Pin FDA UDI
Model / Reference
302204-200 FDA UDI
Description
Cable, Reusable Shielded Mono with Pin FDA UDI

Identifiers

Primary DI / UDI-DI
00840067101230 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electromyographic needle electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 39 Inch FDA UDI

Category: Electromyographic needle electrode, single-use

Cadwell Shielded Cable by Cadwell Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromyographic needle electrode, single-use.

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 7952e32f-769d-485c-b713-813d5ac0809b 35 fields · synced Jun 9, 2026