gudid
Primary ID: 603540AN
FRC POSTEC PLUS (UDI 603540AN)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FRC POSTEC PLUS - Primary ID 603540AN
Device Regulatory Overview
The FRC POSTEC PLUS (Model/Catalog Number: 603540AN) 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
- 603540AN
- Product Code / EMDN
- ELR
- Device Name
- FRC Postec Plus Refill/20 Size 0
- 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 FRC POSTEC PLUS?
The registered manufacturer of record for FRC POSTEC PLUS is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for FRC POSTEC PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 603540AN.
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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