← Back to catalogue

Cadwell Clip-On Lead Wire

FDA UDI

Class II (US FDA UDI)

by Cadwell Industries, Inc.

Identity

Trade Name
Cadwell Clip-On Lead Wire FDA UDI
Generic Name
Electromyographic needle electrode, single-use FDA UDI
Model / Reference
302773-200 FDA UDI

Identifiers

Primary DI / UDI-DI
00840067100318 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 72 Inch FDA UDI

Category: Electromyographic needle electrode, single-use

Cadwell Clip-On Lead Wire 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 8306daff-6948-4c4e-aac0-94f72ac5eb0d 34 fields · synced Jun 9, 2026