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BE PLUS LTM Battery Pack

FDA UDI

Class II (US FDA UDI)

by Eb Neuro Spa

Identity

Trade Name
BE PLUS LTM Battery Pack FDA UDI
Generic Name
Electroencephalograph FDA UDI
Device Name
Battery Pack for EEG Amplifier FDA UDI
Model / Reference
B9100820200 FDA UDI
Description
Battery Pack for EEG Amplifier FDA UDI

Identifiers

Primary DI / UDI-DI
08056446900147 FDA UDI
510(k) Number
K121996 FDA UDI
FDA Product Code
GWL FDA UDI
GMDN Term
Electroencephalograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1835 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

Category: Electroencephalograph

BE PLUS LTM Battery Pack by Eb Neuro Spa — 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
Eb Neuro Spa

Sources (1)

  • FDA UDI c4fdecf1-3a25-4173-92b0-0fa7e411dffa 35 fields · synced May 30, 2026