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Stimulation coil DuoMAG 60BF-NL

FDA UDI

Class II (US FDA UDI)

by DEYMED Diagnostic s.r.o.

Identity

Trade Name
Stimulation coil DuoMAG 60BF-NL FDA UDI
Generic Name
Magnetic neural stimulation system FDA UDI
Device Name
47-655 FDA UDI
Model / Reference
47-655 FDA UDI
Description
47-655 FDA UDI

Identifiers

Catalog Number
47-655 FDA UDI
Primary DI / UDI-DI
08592566476556 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

Stimulation coil DuoMAG 60BF-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

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Manufacturer

Manufacturer
DEYMED Diagnostic s.r.o.

Sources (1)

  • FDA UDI 5e9473be-cb3d-471f-8d56-173dbcee9877 36 fields · synced May 30, 2026