Sensory Roller Set white (UDI 04260203791709)
Manufactured by Novafon Elektromedizinische Geräte GmbH
Device Regulatory Overview
The Sensory Roller Set white (Model/Catalog Number: 7017) is a medical device manufactured by Novafon Elektromedizinische Geräte GmbH. This product is indexed under FDA Product Code / Category Classification Z12069080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7017
- Product Code / EMDN
- Z12069080
- Device Name
- Sensory Roller Set
- Database Sync Date
- 2026-08-09 17:20:11
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 Sensory Roller Set white?
The registered manufacturer of record for Sensory Roller Set white is Novafon Elektromedizinische Geräte GmbH.
What is the Primary UDI-DI identifier for Sensory Roller Set white?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260203791709.
What classification code is assigned to this device?
This device is registered under product classification code Z12069080.
Similar Classification Devices (Z12069080)
Other Devices by Novafon Elektromedizinische Geräte GmbH
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