GUDIDData
eudamed_udi Primary ID: 03760365460358

MANCHESTER 3 AMAGNETIQUE (UDI 03760365460358)

Manufactured by ACIME FRAME

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MANCHESTER 3 AMAGNETIQUE - Primary ID 03760365460358

Device Regulatory Overview

The MANCHESTER 3 AMAGNETIQUE (Model/Catalog Number: MANC035) is a medical device manufactured by ACIME FRAME. This product is indexed under FDA Product Code / Category Classification V080502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MANC035
Product Code / EMDN
V080502
Device Name
MANC-IRM-NI
Database Sync Date
2026-08-09 16:46:36

Full Regulatory Attributes

🔒 Token Gated
{
    "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 MANCHESTER 3 AMAGNETIQUE?

The registered manufacturer of record for MANCHESTER 3 AMAGNETIQUE is ACIME FRAME.

What is the Primary UDI-DI identifier for MANCHESTER 3 AMAGNETIQUE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760365460358.

What classification code is assigned to this device?

This device is registered under product classification code V080502.

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