FRC Postec Plus Refill (UDI 590222AN)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Device Regulatory Overview
The FRC Postec Plus Refill (Model/Catalog Number: 590222AN) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification ELR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 590222AN
- Product Code / EMDN
- ELR
- Device Name
- FRC Postec Plus
- Database Sync Date
- 2026-08-09 09:01:06
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 FRC Postec Plus Refill?
The registered manufacturer of record for FRC Postec Plus Refill is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for FRC Postec Plus Refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 590222AN.
What classification code is assigned to this device?
This device is registered under product classification code ELR.
Similar Classification Devices (ELR)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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