GUDIDData
eudamed_udi Primary ID: D-893875TW

Unspecified Brand (UDI D-893875TW)

Manufactured by MED ITALIA BIOMEDICA S.R.L

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID D-893875TW

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 893875) is a medical device manufactured by MED ITALIA BIOMEDICA S.R.L. This product is indexed under FDA Product Code / Category Classification T0202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
893875
Product Code / EMDN
T0202
Device Name
CORONAROGRAPHY SET
Database Sync Date
2026-08-09 16:30:01

Full Regulatory Attributes

πŸ”’ 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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is MED ITALIA BIOMEDICA S.R.L.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-893875TW.

What classification code is assigned to this device?

This device is registered under product classification code T0202.

Programmatic Export

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

JSON API Endpoint