← Back to catalogue

Liquid cooling DuoMAG NL

FDA UDI

Class II (US FDA UDI)

by DEYMED Diagnostic s.r.o.

Identity

Trade Name
Liquid cooling DuoMAG NL FDA UDI
Generic Name
Magnetic neural stimulation system FDA UDI
Device Name
47-831 FDA UDI
Model / Reference
47-831 FDA UDI
Description
47-831 FDA UDI

Identifiers

Catalog Number
47-831 FDA UDI
Primary DI / UDI-DI
08592566478314 FDA UDI
FDA Product Code
QPL FDA UDI
IPF FDA UDI
GMDN Term
Magnetic neural stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5850 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

No

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: Magnetic neural stimulation system

Liquid cooling DuoMAG NL by DEYMED Diagnostic s.r.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic neural stimulation 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
DEYMED Diagnostic s.r.o.

Sources (1)

  • FDA UDI c009f4e3-7d10-44ca-9703-1835f611ebcb 36 fields · synced May 30, 2026