gudid
Primary ID: P S10
VISIANO 10-1 (UDI P S10)
Manufactured by Derungs Licht AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISIANO 10-1 - Primary ID P S10
Device Regulatory Overview
The VISIANO 10-1 (Model/Catalog Number: P S10) is a medical device manufactured by Derungs Licht AG. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P S10
- Product Code / EMDN
- KZF
- Device Name
- LED Examination Light, 2105359, Pin Mount
- Database Sync Date
- 2026-08-09 09:16:11
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 VISIANO 10-1?
The registered manufacturer of record for VISIANO 10-1 is Derungs Licht AG.
What is the Primary UDI-DI identifier for VISIANO 10-1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P S10.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by Derungs Licht AG
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