Nucleus

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name: Nucleus FDA UDI
Generic Name: Cochlear implant system FDA UDI
Device Name: Cochlear EAC200 Series Speaker Mould Removal Tool FDA UDI
Model / Reference: Z322480 FDA UDI
Description: Cochlear EAC200 Series Speaker Mould Removal Tool FDA UDI

Identifiers

Catalog Number: Z322480 FDA UDI
Primary DI / UDI-DI: 09321502024983 FDA UDI
PMA Number: P130016 FDA UDI
FDA Product Code: PGQ FDA UDI
GMDN Term: Cochlear implant system FDA UDI

Classification

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

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Cochlear implant system

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

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Cleared under the same submission

P130016 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Cochlear

Sources (1)

FDA UDI 65c4c818-4867-4274-8340-60305b69fca0 36 fields · synced Jun 8, 2026