eudamed_udi
Primary ID: 06975662250121
HEKA SOFT (UDI 06975662250121)
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 HEKA SOFT - Primary ID 06975662250121
Device Regulatory Overview
The HEKA SOFT (Model/Catalog Number: VA0913) 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
- VA0913
- Product Code / EMDN
- M040301
- Device Name
- EYE PAD
- Database Sync Date
- 2026-08-09 18:11:17
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HEKA SOFT?
The registered manufacturer of record for HEKA SOFT is Suzhou Vicon Industrial CO., LTD..
What is the Primary UDI-DI identifier for HEKA SOFT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975662250121.
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.
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