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Cochlear™ Nucleus® CI632 cochlear implant with Slim Modiolar electrode

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Cochlear™ Nucleus® CI632 cochlear implant with Slim Modiolar electrode FDA UDI
Generic Name
Cochlear implant system electrode array assembly FDA UDI
Device Name
N/A FDA UDI
Model / Reference
P783831 FDA UDI
Description
N/A FDA UDI

Identifiers

Catalog Number
P783831 FDA UDI
Primary DI / UDI-DI
09321502036580 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant system electrode array assembly FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cochlear implant system electrode array assembly

Cochlear™ Nucleus® CI632 cochlear implant with Slim Modiolar electrode by Cochlear — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cochlear implant system electrode array assembly.

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 8e473871-9183-42d2-8e26-cbd78e244c99 36 fields · synced May 30, 2026