eudamed_udi
Primary ID: 03701160200534
isahead™ (UDI 03701160200534)
Manufactured by MOVE-UP
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for isahead™ - Primary ID 03701160200534
Device Regulatory Overview
The isahead™ (Model/Catalog Number: 0009I4315) is a medical device manufactured by MOVE-UP. This product is indexed under FDA Product Code / Category Classification P090104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0009I4315
- Product Code / EMDN
- P090104010101
- Device Name
- isahead™ Tête humérale Ø 43 mm excentrée 1,5 mm
- Database Sync Date
- 2026-08-09 16:28:54
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 isahead™?
The registered manufacturer of record for isahead™ is MOVE-UP.
What is the Primary UDI-DI identifier for isahead™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701160200534.
What classification code is assigned to this device?
This device is registered under product classification code P090104010101.
Similar Classification Devices (P090104010101)
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