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Cyberonics® Patient Magnet

FDA UDI

Class I (US FDA UDI)

by LivaNova USA, Inc.

Identity

Trade Name
Cyberonics® Patient Magnet FDA UDI
Generic Name
Active implantable device control magnet FDA UDI
Device Name
Patient Magnet FDA UDI
Model / Reference
220 FDA UDI
Description
Patient Magnet FDA UDI

Identifiers

Primary DI / UDI-DI
05425025750252 FDA UDI
510(k) Number
K092364 FDA UDI
FDA Product Code
DTG FDA UDI
GMDN Term
Active implantable device control magnet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.3690 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Active implantable device control magnet

Cyberonics® Patient Magnet by LivaNova USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Active implantable device control magnet.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LivaNova USA, Inc.

Sources (1)

  • FDA UDI 7b4a411a-ffd7-4749-922e-db8d240aab8c 36 fields · synced Jun 8, 2026