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Paradigm

FDA UDI

Class II (US FDA UDI)

by Starkey Laboratories Inc.

Identity

Trade Name
Paradigm FDA UDI
Generic Name
Hearing aid/implant system remote control FDA UDI
Model / Reference
SurfLink Remote Basic (Black) FDA UDI

Identifiers

Catalog Number
60111-000 FDA UDI
Primary DI / UDI-DI
00842318106612 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Hearing aid/implant system remote control 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/implant system remote control

Paradigm by Starkey Laboratories Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hearing aid/implant system remote control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20e91bca-54a0-43ff-9aa9-bb2a31137d1e 33 fields · synced Jun 9, 2026