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Nucleus

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Nucleus FDA UDI
Generic Name
Cochlear implant/auditory brainstem implant peripheral connector FDA UDI
Device Name
Cochlear Nucleus CP900 Series LiteWear Cable (30 cm, Maize) FDA UDI
Model / Reference
Z285951 FDA UDI
Description
Cochlear Nucleus CP900 Series LiteWear Cable (30 cm, Maize) FDA UDI

Identifiers

Catalog Number
Z285951 FDA UDI
Primary DI / UDI-DI
09321502023320 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant/auditory brainstem implant peripheral connector 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

Dimensions & Sizes

Size
Length — 30 Centimeter FDA UDI

Category: Cochlear implant/auditory brainstem implant peripheral connector

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

Similar devices

Also classified as Cochlear implant/auditory brainstem implant peripheral connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cochlear

Sources (1)

  • FDA UDI 14efdf11-6002-4060-8173-1303bf04d4f8 37 fields · synced May 30, 2026