OptraSculpt Pad Refill (UDI 639793AN)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Device Regulatory Overview
The OptraSculpt Pad Refill (Model/Catalog Number: 639793AN) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification KXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 639793AN
- Product Code / EMDN
- KXR
- Device Name
- OptraSculpt Pad Refill
- Database Sync Date
- 2026-08-09 09:01:02
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 OptraSculpt Pad Refill?
The registered manufacturer of record for OptraSculpt Pad Refill is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for OptraSculpt Pad Refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 639793AN.
What classification code is assigned to this device?
This device is registered under product classification code KXR.
Similar Classification Devices (KXR)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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