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Bioprotech Inc.

FDA UDI

Class II (US FDA UDI)

by Bioprotech Inc.

Identity

Trade Name
BIOPROTECH INC. FDA UDI
Generic Name
Electroencephalograph FDA UDI
Device Name
Deep CUP EEG electrode : Disposable, EEG Cup Electrodes. FDA UDI
Model / Reference
DEEG-A-20 FDA UDI
Description
Deep CUP EEG electrode : Disposable, EEG Cup Electrodes. FDA UDI

Identifiers

Primary DI / UDI-DI
08809083941024 FDA UDI
510(k) Number
K153019 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Electroencephalograph 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electroencephalograph

Bioprotech Inc. by Bioprotech Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalograph.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioprotech Inc.

Sources (1)

  • FDA UDI ccf0ed61-3bc8-4db4-b624-3447ac7f7d88 35 fields · synced May 30, 2026