GUDIDData
eudamed_udi Primary ID: 05407007752973

Handpiece For All Inserts (UDI 05407007752973)

Manufactured by Surgi-Tec NV

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Handpiece For All Inserts - Primary ID 05407007752973

Device Regulatory Overview

The Handpiece For All Inserts (Model/Catalog Number: 99-901A) is a medical device manufactured by Surgi-Tec NV. This product is indexed under FDA Product Code / Category Classification L030199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
99-901A
Product Code / EMDN
L030199
Device Name
SURGICAL INSTRUMENTS
Database Sync Date
2026-08-09 16:58:31

Full Regulatory Attributes

๐Ÿ”’ 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 Handpiece For All Inserts?

The registered manufacturer of record for Handpiece For All Inserts is Surgi-Tec NV.

What is the Primary UDI-DI identifier for Handpiece For All Inserts?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05407007752973.

What classification code is assigned to this device?

This device is registered under product classification code L030199.

Programmatic Export

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

JSON API Endpoint