eudamed_udi
Primary ID: 08055712320078
ENF Pro (UDI 08055712320078)
Manufactured by Fast Therapies srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ENF Pro - Primary ID 08055712320078
Device Regulatory Overview
The ENF Pro (Model/Catalog Number: 035) is a medical device manufactured by Fast Therapies srl. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 035
- Product Code / EMDN
- Z120601
- Device Name
- ENF Pro
- Database Sync Date
- 2026-08-09 16:29:22
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 ENF Pro?
The registered manufacturer of record for ENF Pro is Fast Therapies srl.
What is the Primary UDI-DI identifier for ENF Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055712320078.
What classification code is assigned to this device?
This device is registered under product classification code Z120601.
Similar Classification Devices (Z120601)
Other Devices by Fast Therapies srl
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