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SYMFIT 7.0 Package

FDA UDI

Class III (US FDA UDI)

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

Identity

Trade Name
SYMFIT 7.0 Package FDA UDI
Generic Name
Audiometric/hearing device software FDA UDI
Device Name
Fitting Software FDA UDI
Model / Reference
51529 FDA UDI
Description
Fitting Software FDA UDI

Identifiers

Primary DI / UDI-DI
09008738515293 FDA UDI
510(k) Number
FDA Product Code
MPV FDA UDI
PFO FDA UDI
GMDN Term
Audiometric/hearing device software FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
874.3340 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Audiometric/hearing device software

SYMFIT 7.0 Package 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 Audiometric/hearing device software.

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 149a9c0c-6544-4d3d-a7d7-53645e063ac1 35 fields · synced May 30, 2026