gudid Primary ID: (precious pink)

Phonak CROS E-R (UDI (precious pink))

Manufactured by Sonova AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phonak CROS E-R (Model/Catalog Number: (precious pink)) is a medical device manufactured by Sonova AG. This product is indexed under FDA Product Code / Category Classification OSM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: (precious pink)
Product Code / EMDN: OSM
Device Name
Database Sync Date: 2026-08-09 09:19:56

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 Phonak CROS E-R?

The registered manufacturer of record for Phonak CROS E-R is Sonova AG.

What is the Primary UDI-DI identifier for Phonak CROS E-R?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is (precious pink).

What classification code is assigned to this device?

This device is registered under product classification code OSM.

Similar Classification Devices (OSM)

Other Devices by Sonova AG

Programmatic Export

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

JSON API Endpoint