eudamed_udi
Primary ID: 06222012070718
Ortho (UDI 06222012070718)
Manufactured by Miracle Medical Industries
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ortho - Primary ID 06222012070718
Device Regulatory Overview
The Ortho (Model/Catalog Number: 6222012070718) is a medical device manufactured by Miracle Medical Industries. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6222012070718
- Product Code / EMDN
- Y061218
- Device Name
- Ankle Brace Criss Cross M
- Database Sync Date
- 2026-08-09 16:48:22
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 Ortho?
The registered manufacturer of record for Ortho is Miracle Medical Industries.
What is the Primary UDI-DI identifier for Ortho?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06222012070718.
What classification code is assigned to this device?
This device is registered under product classification code Y061218.
Similar Classification Devices (Y061218)
Other Devices by Miracle Medical Industries
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