← Back to catalogue

Widex

FDA UDI

Class II (US FDA UDI)

by Widex A/S

Identity

Trade Name
Widex FDA UDI
Generic Name
Hearing aid wireless-fitting computer-aided set FDA UDI
Device Name
ProgLink (Black ) FDA UDI
Model / Reference
ProgLink FDA UDI
Description
ProgLink (Black ) FDA UDI

Identifiers

Catalog Number
8 917 0200 000 FDA UDI
Primary DI / UDI-DI
05706069409017 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Hearing aid wireless-fitting computer-aided set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3305 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hearing aid wireless-fitting computer-aided set

Widex by Widex A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hearing aid wireless-fitting computer-aided set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Widex A/S

Sources (1)

  • FDA UDI b9d7c6d1-abcf-4f50-b4d8-c29603259b0c 35 fields · synced May 30, 2026