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Cochlear™ Baha® 6 Max Sound Processor, Silver

FDA UDI

Class II (US FDA UDI)

by Cochlear Bone Anchored Solutions AB

Identity

Trade Name
Cochlear™ Baha® 6 Max Sound Processor, Silver FDA UDI
Generic Name
Bone-conduction hearing implant system sound processor/vibrator FDA UDI
Model / Reference
P1668391 FDA UDI

Identifiers

Catalog Number
P1668391 FDA UDI
Primary DI / UDI-DI
09321502052030 FDA UDI
510(k) Number
K202048 FDA UDI
FDA Product Code
LXB FDA UDI
GMDN Term
Bone-conduction hearing implant system sound processor/vibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3302 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bone-conduction hearing implant system sound processor/vibrator

Cochlear™ Baha® 6 Max Sound Processor, Silver by Cochlear Bone Anchored Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-conduction hearing implant system sound processor/vibrator.

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 4bca5b9a-d392-4392-b6c0-16697cc46b60 35 fields · synced May 30, 2026