eudamed_udi
Primary ID: 06974686059840
Eye Pad (UDI 06974686059840)
Manufactured by Yiwu Ori-Power Medtech Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eye Pad - Primary ID 06974686059840
Device Regulatory Overview
The Eye Pad (Model/Catalog Number: ENEPX2BA001) is a medical device manufactured by Yiwu Ori-Power Medtech 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
- ENEPX2BA001
- Product Code / EMDN
- M040301
- Device Name
- Eye Pad
- Database Sync Date
- 2026-08-09 16:30:25
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 Eye Pad?
The registered manufacturer of record for Eye Pad is Yiwu Ori-Power Medtech Co.,Ltd..
What is the Primary UDI-DI identifier for Eye Pad?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974686059840.
What classification code is assigned to this device?
This device is registered under product classification code M040301.
Similar Classification Devices (M040301)
Other Devices by Yiwu Ori-Power Medtech Co.,Ltd.
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