equator LCT (UDI +D932120300121Z)
Manufactured by Dent-A-Pharm Produktionsgesellschaft mbH
Device Regulatory Overview
The equator LCT (Model/Catalog Number: 12030012) is a medical device manufactured by Dent-A-Pharm Produktionsgesellschaft mbH. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12030012
- Product Code / EMDN
- Q010503
- Device Name
- Light curing tray material
- Database Sync Date
- 2026-08-09 16:29:03
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 equator LCT?
The registered manufacturer of record for equator LCT is Dent-A-Pharm Produktionsgesellschaft mbH.
What is the Primary UDI-DI identifier for equator LCT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D932120300121Z.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
Other Devices by Dent-A-Pharm Produktionsgesellschaft mbH
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