gudid
Primary ID: 603541AN
FRC POSTEC PLUS (UDI 603541AN)
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 603541AN
Device Regulatory Overview
The FRC POSTEC PLUS (Model/Catalog Number: 603541AN) 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
- 603541AN
- Product Code / EMDN
- ELR
- Device Name
- FRC Postec Plus Refill/5 Size 0
- Database Sync Date
- 2026-08-09 09:01:02
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 603541AN.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint