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Mi1210 SYNCHRONY ST +MEDIUM

FDA UDI

Class III (US FDA UDI)

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

Identity

Trade Name
Mi1210 SYNCHRONY ST +MEDIUM FDA UDI
Generic Name
Cochlear implant system electrode array assembly FDA UDI
Device Name
Cochlear Implant FDA UDI
Model / Reference
33183 FDA UDI
Description
Cochlear Implant FDA UDI

Identifiers

Catalog Number
33334 FDA UDI
Primary DI / UDI-DI
09008737331832 FDA UDI
PMA Number
P000025 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

Mi1210 SYNCHRONY ST +MEDIUM 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 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

Sources (1)

  • FDA UDI f3dc4e0f-1eb4-4c52-b2be-7c0e8144326e 37 fields · synced Jun 6, 2026