gudid
Primary ID: PCSRSEK1
CLEARSPLINT (UDI PCSRSEK1)
Manufactured by ASTRON DENTAL CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CLEARSPLINT - Primary ID PCSRSEK1
Device Regulatory Overview
The CLEARSPLINT (Model/Catalog Number: PCSRSEK1) is a medical device manufactured by ASTRON DENTAL CORPORATION. This product is indexed under FDA Product Code / Category Classification MQC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PCSRSEK1
- Product Code / EMDN
- MQC
- Device Name
- DENTURE MATERIAL - SUPER ECONO KIT - PACKAGE 960 GRAMS POWDER/3 EACH 240 GRAMS LIQUID
- Database Sync Date
- 2026-08-09 09:05:41
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 CLEARSPLINT?
The registered manufacturer of record for CLEARSPLINT is ASTRON DENTAL CORPORATION.
What is the Primary UDI-DI identifier for CLEARSPLINT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PCSRSEK1.
What classification code is assigned to this device?
This device is registered under product classification code MQC.
Similar Classification Devices (MQC)
Other Devices by ASTRON DENTAL CORPORATION
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