← Back to catalogue

Cervello 32

FDA UDI

Class II (US FDA UDI)

by Blackrock Neuromed, Llc

Identity

Trade Name
CERVELLO 32 FDA UDI
Generic Name
Electroencephalography telemetric monitoring system FDA UDI
Device Name
Cervello 32 LTM / Ambulatory Headbox, needs Jack Box - Bluetooth Model FDA UDI
Model / Reference
7511 FDA UDI
Description
Cervello 32 LTM / Ambulatory Headbox, needs Jack Box - Bluetooth Model FDA UDI

Identifiers

Catalog Number
7511 FDA UDI
Primary DI / UDI-DI
00850154007000 FDA UDI
FDA Product Code
GWK FDA UDI
OLV FDA UDI
GWQ FDA UDI
GWL FDA UDI
GMDN Term
Electroencephalography telemetric monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1845 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

No

FDA UDI

Category: Electroencephalography telemetric monitoring system

Cervello 32 by Blackrock Neuromed, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalography telemetric monitoring system.

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

Manufacturer
Blackrock Neuromed, Llc

Sources (1)

  • FDA UDI d5b38ba6-e369-42d3-b124-b1e1185da50a 35 fields · synced Jun 8, 2026