GUDIDData
gudid Primary ID: 2018-0030

Silicone Thoracic Drain, S Type (UDI 2018-0030)

Manufactured by FORTUNE MEDICAL INSTRUMENT CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Silicone Thoracic Drain, S Type - Primary ID 2018-0030

Device Regulatory Overview

The Silicone Thoracic Drain, S Type (Model/Catalog Number: 2018-0030) is a medical device manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. This product is indexed under FDA Product Code / Category Classification GBS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2018-0030
Product Code / EMDN
GBS
Device Name
Database Sync Date
2026-08-09 09:29:18

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 Silicone Thoracic Drain, S Type?

The registered manufacturer of record for Silicone Thoracic Drain, S Type is FORTUNE MEDICAL INSTRUMENT CORP..

What is the Primary UDI-DI identifier for Silicone Thoracic Drain, S Type?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2018-0030.

What classification code is assigned to this device?

This device is registered under product classification code GBS.

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