eudamed_udi
Primary ID: 06971819180303
KEFFORT (UDI 06971819180303)
Manufactured by Netop Industrial Company Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KEFFORT - Primary ID 06971819180303
Device Regulatory Overview
The KEFFORT (Model/Catalog Number: MC-100A) is a medical device manufactured by Netop Industrial Company Limited. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MC-100A
- Product Code / EMDN
- Z12062801
- Device Name
- Electrical Neuromuscular stimulator for urinary incontinence treatment
- Database Sync Date
- 2026-08-09 16:29:47
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 KEFFORT?
The registered manufacturer of record for KEFFORT is Netop Industrial Company Limited.
What is the Primary UDI-DI identifier for KEFFORT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971819180303.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by Netop Industrial Company Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint