eudamed_udi Primary ID: 03701160201135

isasphere™ (UDI 03701160201135)

Manufactured by MOVE-UP

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The isasphere™ (Model/Catalog Number: 0015I3902) is a medical device manufactured by MOVE-UP. This product is indexed under FDA Product Code / Category Classification P09010303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0015I3902
Product Code / EMDN: P09010303
Device Name: isasphere™Glénosphère Ø 39 mm excentrée 2 mm
Database Sync Date: 2026-08-09 16:28:56

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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Frequently Asked Questions

Who is the primary manufacturer of isasphere™?

The registered manufacturer of record for isasphere™ is MOVE-UP.

What is the Primary UDI-DI identifier for isasphere™?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701160201135.

What classification code is assigned to this device?

This device is registered under product classification code P09010303.

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