GUDIDData
eudamed_udi Primary ID: 08718657211442

Curan Man (UDI 08718657211442)

Manufactured by Curan Medical BV

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Curan Man - Primary ID 08718657211442

Device Regulatory Overview

The Curan Man (Model/Catalog Number: CM16) is a medical device manufactured by Curan Medical BV. This product is indexed under FDA Product Code / Category Classification U01010501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CM16
Product Code / EMDN
U01010501
Device Name
Curan Man
Database Sync Date
2026-08-09 16:29:50

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 Curan Man?

The registered manufacturer of record for Curan Man is Curan Medical BV.

What is the Primary UDI-DI identifier for Curan Man?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08718657211442.

What classification code is assigned to this device?

This device is registered under product classification code U01010501.

Programmatic Export

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

JSON API Endpoint