gudid
Primary ID: 970-0058B
Master Series (UDI 970-0058B)
Manufactured by AMERICAN ORTHODONTICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Master Series - Primary ID 970-0058B
Device Regulatory Overview
The Master Series (Model/Catalog Number: 970-0058B) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification EJF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 970-0058B
- Product Code / EMDN
- EJF
- Device Name
- DB BKT MASTER HGW LR 2ND BIC 022 T-22 A=0 R4D 197 PAD W/HK DIST
- 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 Master Series?
The registered manufacturer of record for Master Series is AMERICAN ORTHODONTICS CORPORATION.
What is the Primary UDI-DI identifier for Master Series?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 970-0058B.
What classification code is assigned to this device?
This device is registered under product classification code EJF.
Similar Classification Devices (EJF)
Other Devices by AMERICAN ORTHODONTICS CORPORATION
Programmatic Export
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