GUDIDData
gudid Primary ID: Ascend

SyncLync (UDI Ascend)

Manufactured by audifon GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SyncLync - Primary ID Ascend

Device Regulatory Overview

The SyncLync (Model/Catalog Number: Ascend) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification OSM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Ascend
Product Code / EMDN
OSM
Device Name
SyncLync Ascend+ -- anthrazit
Database Sync Date
2026-08-09 09:23:55

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of SyncLync?

The registered manufacturer of record for SyncLync is audifon GmbH & Co. KG.

What is the Primary UDI-DI identifier for SyncLync?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Ascend.

What classification code is assigned to this device?

This device is registered under product classification code OSM.

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