GUDIDData
eudamed_udi Primary ID: D-SMR355JP

ECTphan™ (UDI D-SMR355JP)

Manufactured by Phantom Laboratory

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ECTphan™ - Primary ID D-SMR355JP

Device Regulatory Overview

The ECTphan™ (Model/Catalog Number: SMR355) is a medical device manufactured by Phantom Laboratory. This product is indexed under FDA Product Code / Category Classification Z119080 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SMR355
Product Code / EMDN
Z119080
Device Name
SMR355
Database Sync Date
2026-08-09 18:26:21

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 ECTphan™?

The registered manufacturer of record for ECTphan™ is Phantom Laboratory.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-SMR355JP.

What classification code is assigned to this device?

This device is registered under product classification code Z119080.

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