eudamed_udi
Primary ID: 06222012004263
Miracle (UDI 06222012004263)
Manufactured by Miracle Medical Industries
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Miracle - Primary ID 06222012004263
Device Regulatory Overview
The Miracle (Model/Catalog Number: 6222012004263) is a medical device manufactured by Miracle Medical Industries. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6222012004263
- Product Code / EMDN
- Y060612
- Device Name
- WRIST SPLINT WITH STRAP size XS
- Database Sync Date
- 2026-08-09 16:29:10
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Miracle?
The registered manufacturer of record for Miracle is Miracle Medical Industries.
What is the Primary UDI-DI identifier for Miracle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06222012004263.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
Other Devices by Miracle Medical Industries
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint