eudamed_udi
Primary ID: 08721593324008
Reforter (UDI 08721593324008)
Manufactured by Hapticlink Technologies B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reforter - Primary ID 08721593324008
Device Regulatory Overview
The Reforter (Model/Catalog Number: HLP001) is a medical device manufactured by Hapticlink Technologies B.V.. This product is indexed under FDA Product Code / Category Classification Z120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HLP001
- Product Code / EMDN
- Z120602
- Device Name
- Reforter
- Database Sync Date
- 2026-08-09 16:29:18
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 Reforter?
The registered manufacturer of record for Reforter is Hapticlink Technologies B.V..
What is the Primary UDI-DI identifier for Reforter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08721593324008.
What classification code is assigned to this device?
This device is registered under product classification code Z120602.
Similar Classification Devices (Z120602)
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