GUDIDData
gudid Primary ID: M004PM4790K20

IntellaTip MiFi XP (UDI M004PM4790K20)

Manufactured by BOSTON SCIENTIFIC CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IntellaTip MiFi XP - Primary ID M004PM4790K20

Device Regulatory Overview

The IntellaTip MiFi XP (Model/Catalog Number: M004PM4790K20) is a medical device manufactured by BOSTON SCIENTIFIC CORPORATION. This product is indexed under FDA Product Code / Category Classification OAD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M004PM4790K20
Product Code / EMDN
OAD
Device Name
Temperature Ablation Catheter
Database Sync Date
2026-08-09 09:26:56

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 IntellaTip MiFi XP?

The registered manufacturer of record for IntellaTip MiFi XP is BOSTON SCIENTIFIC CORPORATION.

What is the Primary UDI-DI identifier for IntellaTip MiFi XP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M004PM4790K20.

What classification code is assigned to this device?

This device is registered under product classification code OAD.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint