gudid
Primary ID: 0302
Unilateral casting (UDI 0302)
Manufactured by Digital Dental Laboratories, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unilateral casting - Primary ID 0302
Device Regulatory Overview
The Unilateral casting (Model/Catalog Number: 0302) is a medical device manufactured by Digital Dental Laboratories, Inc. This product is indexed under FDA Product Code / Category Classification NSK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0302
- Product Code / EMDN
- NSK
- Device Name
- Database Sync Date
- 2026-08-09 09:12:25
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 Unilateral casting?
The registered manufacturer of record for Unilateral casting is Digital Dental Laboratories, Inc.
What is the Primary UDI-DI identifier for Unilateral casting?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0302.
What classification code is assigned to this device?
This device is registered under product classification code NSK.
Similar Classification Devices (NSK)
Other Devices by Digital Dental Laboratories, Inc
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