gudid
Primary ID: 1kg ; Color:A1
printodent GR-21.1 Try-In (UDI 1kg ; Color:A1)
Manufactured by pro3dure medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for printodent GR-21.1 Try-In - Primary ID 1kg ; Color:A1
Device Regulatory Overview
The printodent GR-21.1 Try-In (Model/Catalog Number: 1kg ; Color:A1) is a medical device manufactured by pro3dure medical GmbH. This product is indexed under FDA Product Code / Category Classification EEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1kg ; Color:A1
- Product Code / EMDN
- EEA
- Device Name
- printodent GR-21.1 Try-In1kg ; Color:A1
- Database Sync Date
- 2026-08-09 09:51:23
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 printodent GR-21.1 Try-In?
The registered manufacturer of record for printodent GR-21.1 Try-In is pro3dure medical GmbH.
What is the Primary UDI-DI identifier for printodent GR-21.1 Try-In?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1kg ; Color:A1.
What classification code is assigned to this device?
This device is registered under product classification code EEA.
Similar Classification Devices (EEA)
Other Devices by pro3dure medical GmbH
Programmatic Export
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