Kit Cutting guide Regular Non-Engaging (UDI 08435566617010)
Manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.
Device Regulatory Overview
The Kit Cutting guide Regular Non-Engaging (Model/Catalog Number: IPD/KT-IR-01) is a medical device manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.. This product is indexed under FDA Product Code / Category Classification Q010280,Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IPD/KT-IR-01
- Product Code / EMDN
- Q010280,Q010299
- Device Name
- Cutting guide
- Database Sync Date
- 2026-08-09 16:28:59
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 Kit Cutting guide Regular Non-Engaging?
The registered manufacturer of record for Kit Cutting guide Regular Non-Engaging is IMPLANT PROTESIS DENTAL 2004 S.L..
What is the Primary UDI-DI identifier for Kit Cutting guide Regular Non-Engaging?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435566617010.
What classification code is assigned to this device?
This device is registered under product classification code Q010280,Q010299.
Similar Classification Devices (Q010280,Q010299)
Other Devices by IMPLANT PROTESIS DENTAL 2004 S.L.
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