gudid Primary ID: AMPLI-MINI E 3|7S RITE-R

AMPLIFON (UDI AMPLI-MINI E 3|7S RITE-R)

Manufactured by Starkey Laboratories, Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The AMPLIFON (Model/Catalog Number: AMPLI-MINI E 3|7S RITE-R) is a medical device manufactured by Starkey Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AMPLI-MINI E 3|7S RITE-R
Product Code / EMDN: KLW
Device Name
Database Sync Date: 2026-08-09 09:07:49

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of AMPLIFON?

The registered manufacturer of record for AMPLIFON is Starkey Laboratories, Inc..

What is the Primary UDI-DI identifier for AMPLIFON?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AMPLI-MINI E 3|7S RITE-R.

What classification code is assigned to this device?

This device is registered under product classification code KLW.

Similar Classification Devices (KLW)

Other Devices by Starkey Laboratories, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint