GUDIDData
eudamed_udi Primary ID: 06974998880194

MAIN MEDITECH (UDI 06974998880194)

Manufactured by Main MediTech Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAIN MEDITECH - Primary ID 06974998880194

Device Regulatory Overview

The MAIN MEDITECH (Model/Catalog Number: SL-7S) is a medical device manufactured by Main MediTech Co., Ltd. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SL-7S
Product Code / EMDN
Q0299
Device Name
Slit Lamp
Database Sync Date
2026-08-09 16:28:53

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 MAIN MEDITECH?

The registered manufacturer of record for MAIN MEDITECH is Main MediTech Co., Ltd.

What is the Primary UDI-DI identifier for MAIN MEDITECH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974998880194.

What classification code is assigned to this device?

This device is registered under product classification code Q0299.

Programmatic Export

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

JSON API Endpoint