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Cerebrotech Fluids Monitor

FDA UDI

Class II (US FDA UDI)

by Cerebrotech Medical Systems, Inc.

Identity

Trade Name
Cerebrotech Fluids Monitor FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Device Name
CMS 5000 Fluids Monitor FDA UDI
Model / Reference
5000 FDA UDI
Description
CMS 5000 Fluids Monitor FDA UDI

Identifiers

Primary DI / UDI-DI
00861714000355 FDA UDI
FDA Product Code
MNW FDA UDI
GMDN Term
Bioelectrical body composition analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bioelectrical body composition analyser

Cerebrotech Fluids Monitor by Cerebrotech Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bioelectrical body composition analyser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f8597fd-b41a-4749-ab7e-2cd3bfc0e05d 33 fields · synced May 30, 2026