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BCI 602 Kit

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
BCI 602 Kit FDA UDI
Generic Name
Implantable vibrator bone-conduction hearing implant system FDA UDI
Device Name
Bone Conduction Implant Kit FDA UDI
Model / Reference
52483 FDA UDI
Description
Bone Conduction Implant Kit FDA UDI

Identifiers

Primary DI / UDI-DI
09008737524838 FDA UDI
FDA Product Code
PFO FDA UDI
GMDN Term
Implantable vibrator bone-conduction hearing implant system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3340 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Implantable vibrator bone-conduction hearing implant system

BCI 602 Kit by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable vibrator bone-conduction hearing implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

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

Sources (1)

  • FDA UDI dcd5f0ae-eed2-43f0-b332-5f4173cf5bcb 35 fields · synced May 30, 2026