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Cadwell Single Disc Electrode

FDA UDI

Class II (US FDA UDI)

by Cadwell Industries, Inc.

Identity

Trade Name
Cadwell Single Disc Electrode FDA UDI
Generic Name
Analytical scalp electrode, single-use FDA UDI
Model / Reference
302135-200 FDA UDI

Identifiers

Primary DI / UDI-DI
00840067101032 FDA UDI
510(k) Number
K933802 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical scalp electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 24 Inch FDA UDI

Category: Analytical scalp electrode, single-use

Cadwell Single Disc Electrode by Cadwell Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp electrode, single-use.

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 80efb2dc-396a-4832-9797-17a7bfda2df8 35 fields · synced Jun 9, 2026