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Cochlear™ Hugfit™

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Cochlear™ Hugfit™ FDA UDI
Generic Name
Cochlear implant/auditory brainstem implant sound processor earhook FDA UDI
Device Name
Extra Small FDA UDI
Model / Reference
Z544854 FDA UDI
Description
Extra Small FDA UDI

Identifiers

Catalog Number
Z544854 FDA UDI
Primary DI / UDI-DI
09321502035200 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant/auditory brainstem implant sound processor earhook 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
MRI Safety
MR Unsafe FDA UDI

Category: Cochlear implant/auditory brainstem implant sound processor earhook

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

Similar devices

Also classified as Cochlear implant/auditory brainstem implant sound processor earhook.

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 c373ea5a-9a79-4b7d-ba1b-1f202510421d 36 fields · synced May 31, 2026