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BE Micro Headbox

FDA UDI

Class II (US FDA UDI)

by Eb Neuro Spa

Identity

Trade Name
BE Micro Headbox FDA UDI
Generic Name
Electroencephalographic ambulatory recorder FDA UDI
Device Name
Patient-interface for EEG ambulatory recorder FDA UDI
Model / Reference
B9630073000 FDA UDI
Description
Patient-interface for EEG ambulatory recorder FDA UDI

Identifiers

Primary DI / UDI-DI
08056446900055 FDA UDI
FDA Product Code
MNR FDA UDI
GWQ FDA UDI
GWL FDA UDI
OLV FDA UDI
GMDN Term
Electroencephalographic ambulatory recorder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
882.1400 FDA UDI
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electroencephalographic ambulatory recorder

BE Micro Headbox by Eb Neuro Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalographic ambulatory recorder.

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 8dce03b5-006d-4c05-bc05-b2484ecb6aa4 34 fields · synced May 31, 2026