gudid
Primary ID: SDIA 512-0
NA (UDI SDIA 512-0)
Manufactured by Nobel Biocare AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID SDIA 512-0
Device Regulatory Overview
The NA (Model/Catalog Number: SDIA 512-0) is a medical device manufactured by Nobel Biocare AB. This product is indexed under FDA Product Code / Category Classification DZI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SDIA 512-0
- Product Code / EMDN
- DZI
- Device Name
- Screw tap 4 mm 7-13 mm
- Database Sync Date
- 2026-08-09 09:10:27
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 NA?
The registered manufacturer of record for NA is Nobel Biocare AB.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SDIA 512-0.
What classification code is assigned to this device?
This device is registered under product classification code DZI.
Similar Classification Devices (DZI)
Other Devices by Nobel Biocare AB
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