GUDIDData
gudid Primary ID: TY2016

Themy (UDI TY2016)

Manufactured by M.D.L. S.R.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Themy - Primary ID TY2016

Device Regulatory Overview

The Themy (Model/Catalog Number: TY2016) is a medical device manufactured by M.D.L. S.R.L.. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TY2016
Product Code / EMDN
FCG
Device Name
5 CS- THEMY AUTOMATIC NEEDLE20Gx160mm FOR SOFT TISSUE BIOPSYNOTCH OF 20 mm
Database Sync Date
2026-08-09 09:04:30

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 Themy?

The registered manufacturer of record for Themy is M.D.L. S.R.L..

What is the Primary UDI-DI identifier for Themy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TY2016.

What classification code is assigned to this device?

This device is registered under product classification code FCG.

Programmatic Export

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

JSON API Endpoint