eudamed_udi
Primary ID: 06975662250619
PDL (UDI 06975662250619)
Manufactured by Suzhou Vicon Industrial CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PDL - Primary ID 06975662250619
Device Regulatory Overview
The PDL (Model/Catalog Number: PC-EPD) is a medical device manufactured by Suzhou Vicon Industrial CO., LTD.. This product is indexed under FDA Product Code / Category Classification M040301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PC-EPD
- Product Code / EMDN
- M040301
- Device Name
- EYE PAD
- Database Sync Date
- 2026-08-09 18:00:20
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 PDL?
The registered manufacturer of record for PDL is Suzhou Vicon Industrial CO., LTD..
What is the Primary UDI-DI identifier for PDL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975662250619.
What classification code is assigned to this device?
This device is registered under product classification code M040301.
Similar Classification Devices (M040301)
Other Devices by Suzhou Vicon Industrial CO., LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint