gudid
Primary ID: 004-18-029448HM
ifit (UDI 004-18-029448HM)
Manufactured by AMERICAN ORTHODONTICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ifit - Primary ID 004-18-029448HM
Device Regulatory Overview
The ifit (Model/Catalog Number: 004-18-029448HM) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification DZD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 004-18-029448HM
- Product Code / EMDN
- DZD
- Device Name
- WELD TUBE IFIT UR 1ST MOL 018 CONV T-10 R10D 3.9MM W/HK
- 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 ifit?
The registered manufacturer of record for ifit is AMERICAN ORTHODONTICS CORPORATION.
What is the Primary UDI-DI identifier for ifit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 004-18-029448HM.
What classification code is assigned to this device?
This device is registered under product classification code DZD.
Similar Classification Devices (DZD)
Other Devices by AMERICAN ORTHODONTICS CORPORATION
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