Cerec Ti Base Engaging Ø 3,4 H 0.5 (UDI 08435566628061)
Manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.
Device Regulatory Overview
The Cerec Ti Base Engaging Ø 3,4 H 0.5 (Model/Catalog Number: IPD/BB-IN-00/SI) is a medical device manufactured by IMPLANT PROTESIS DENTAL 2004 S.L.. This product is indexed under FDA Product Code / Category Classification Q01020602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IPD/BB-IN-00/SI
- Product Code / EMDN
- Q01020602
- Device Name
- Hollow Screw System ; Custom Interface System ; Cerec Sirona Ti Base System
- Database Sync Date
- 2026-08-09 16:30:01
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 Cerec Ti Base Engaging Ø 3,4 H 0.5?
The registered manufacturer of record for Cerec Ti Base Engaging Ø 3,4 H 0.5 is IMPLANT PROTESIS DENTAL 2004 S.L..
What is the Primary UDI-DI identifier for Cerec Ti Base Engaging Ø 3,4 H 0.5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435566628061.
What classification code is assigned to this device?
This device is registered under product classification code Q01020602.
Similar Classification Devices (Q01020602)
Other Devices by IMPLANT PROTESIS DENTAL 2004 S.L.
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