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ADHEAR Audio Processor, Model 701, Test Device

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
ADHEAR Audio Processor, Model 701, Test Device FDA UDI
Generic Name
Bone-conduction hearing aid, head-worn FDA UDI
Device Name
Audio Processor FDA UDI
Model / Reference
34688 FDA UDI
Description
Audio Processor FDA UDI

Identifiers

Primary DI / UDI-DI
09008737346881 FDA UDI
510(k) Number
K172460 FDA UDI
FDA Product Code
LXB FDA UDI
GMDN Term
Bone-conduction hearing aid, head-worn 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Bone-conduction hearing aid, head-worn

ADHEAR Audio Processor, Model 701, Test Device by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bone-conduction hearing aid, head-worn.

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 3f47d5a9-bc97-4ece-bdcf-8c13c56946c0 36 fields · synced May 30, 2026