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Nucleus

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Nucleus FDA UDI
Generic Name
Secondary battery FDA UDI
Device Name
CR200 SERIES BATTERY (CR210) FDA UDI
Model / Reference
Z322699 FDA UDI
Description
CR200 SERIES BATTERY (CR210) FDA UDI

Identifiers

Catalog Number
Z322699 FDA UDI
Primary DI / UDI-DI
09321502024549 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Secondary battery 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

No

FDA UDI

Category: Secondary battery

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

Similar devices

Also classified as Secondary battery.

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 fba0d1ca-5c48-44b9-a2e3-56f2c4ea831a 36 fields · synced May 30, 2026