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Nucleus

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Nucleus FDA UDI
Generic Name
Cochlear implant dummy magnet FDA UDI
Device Name
CI500 Series Non-Magnetic Plug FDA UDI
Model / Reference
Z146624 FDA UDI
Description
CI500 Series Non-Magnetic Plug FDA UDI

Identifiers

Catalog Number
Z146624 FDA UDI
Primary DI / UDI-DI
09321502018395 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant dummy magnet FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Cochlear implant dummy magnet

Nucleus by Cochlear — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cochlear implant dummy magnet.

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 2f923d48-2c3c-4673-aed6-3603e06b6b02 36 fields · synced Jun 1, 2026