eudamed_udi Primary ID: 06937036407661

Lightproof Extension Set (UDI 06937036407661)

Manufactured by MEDCAPTAIN LIFE SCIENCE CO., LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lightproof Extension Set (Model/Catalog Number: /) is a medical device manufactured by MEDCAPTAIN LIFE SCIENCE CO., LTD.. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: /
Product Code / EMDN: A03020101
Device Name: Lightproof Extension Set
Database Sync Date: 2026-08-09 16:29:05

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 Lightproof Extension Set?

The registered manufacturer of record for Lightproof Extension Set is MEDCAPTAIN LIFE SCIENCE CO., LTD..

What is the Primary UDI-DI identifier for Lightproof Extension Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06937036407661.

What classification code is assigned to this device?

This device is registered under product classification code A03020101.

Similar Classification Devices (A03020101)

Other Devices by MEDCAPTAIN LIFE SCIENCE CO., LTD.

Programmatic Export

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

JSON API Endpoint