EASYSCOPE (UDI V3.10 USB COM)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The EASYSCOPE (Model/Catalog Number: V3.10 USB COM) is a medical device manufactured by MICROPORT CRM SRL. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: V3.10 USB COM
Product Code / EMDN: DQK
Device Name
Database Sync Date: 2026-08-09 09:05:06

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 EASYSCOPE?

The registered manufacturer of record for EASYSCOPE is MICROPORT CRM SRL.

What is the Primary UDI-DI identifier for EASYSCOPE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V3.10 USB COM.

What classification code is assigned to this device?

This device is registered under product classification code DQK.

Similar Classification Devices (DQK)

Other Devices by MICROPORT CRM SRL

Programmatic Export

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

JSON API Endpoint