eudamed_udi
Primary ID: +D910GDP0
Autoclave iClave 24 Printer (UDI +D910GDP0)
Manufactured by NSK Dental Italy S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Autoclave iClave 24 Printer - Primary ID +D910GDP0
Device Regulatory Overview
The Autoclave iClave 24 Printer (Model/Catalog Number: 92412B0100P) is a medical device manufactured by NSK Dental Italy S.r.l.. This product is indexed under FDA Product Code / Category Classification Z12011305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 92412B0100P
- Product Code / EMDN
- Z12011305
- Device Name
- Autoclave iClave 18/24 - DXPclave 18/24
- Database Sync Date
- 2026-08-09 16:45:39
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 Autoclave iClave 24 Printer?
The registered manufacturer of record for Autoclave iClave 24 Printer is NSK Dental Italy S.r.l..
What is the Primary UDI-DI identifier for Autoclave iClave 24 Printer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D910GDP0.
What classification code is assigned to this device?
This device is registered under product classification code Z12011305.
Similar Classification Devices (Z12011305)
Other Devices by NSK Dental Italy S.r.l.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint