gudid
Primary ID: 845-3U-2020
Beta Titanium Wire (UDI 845-3U-2020)
Manufactured by AMERICAN ORTHODONTICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Beta Titanium Wire - Primary ID 845-3U-2020
Device Regulatory Overview
The Beta Titanium Wire (Model/Catalog Number: 845-3U-2020) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification DZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 845-3U-2020
- Product Code / EMDN
- DZC
- Device Name
- WIRE B-TI FORM III UPPER 020X020 10/PK
- Database Sync Date
- 2026-08-09 09:00:41
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 Beta Titanium Wire?
The registered manufacturer of record for Beta Titanium Wire is AMERICAN ORTHODONTICS CORPORATION.
What is the Primary UDI-DI identifier for Beta Titanium Wire?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 845-3U-2020.
What classification code is assigned to this device?
This device is registered under product classification code DZC.
Similar Classification Devices (DZC)
Other Devices by AMERICAN ORTHODONTICS CORPORATION
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