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SONNET 3 (Me1713) White

FDA UDI

Class III (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name
SONNET 3 (Me1713) White FDA UDI
Generic Name
Cochlear implant/auditory brainstem implant sound processor FDA UDI
Device Name
Audio Processor FDA UDI
Model / Reference
43620 FDA UDI
Description
Audio Processor FDA UDI

Identifiers

Primary DI / UDI-DI
09008737436209 FDA UDI
PMA Number
P000025 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant/auditory brainstem implant sound processor 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cochlear implant/auditory brainstem implant sound processor

SONNET 3 (Me1713) White by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cca61847-57d9-4505-9a40-9487041020ab 36 fields · synced May 30, 2026