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Cochlear™ Magnet Reverse Polarity

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Cochlear™ Magnet Reverse Polarity FDA UDI
Generic Name
Hearing implant system external magnet, reusable FDA UDI
Device Name
Silver, 5(R) FDA UDI
Model / Reference
P1840753 FDA UDI
Description
Silver, 5(R) FDA UDI

Identifiers

Catalog Number
P1840753 FDA UDI
Primary DI / UDI-DI
09321502064255 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Hearing implant system external magnet, reusable FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Hearing implant system external magnet, reusable

Cochlear™ Magnet Reverse Polarity by Cochlear — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hearing implant system external magnet, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cochlear

Sources (1)

  • FDA UDI c65264f9-9f48-4b74-9c75-00b8d196667f 36 fields · synced Jun 8, 2026