GUDIDData
gudid Primary ID: 2015-9621J

Silicone Endo Drain Kit (J Connector+Trocar) (UDI 2015-9621J)

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 Endo Drain Kit (J Connector+Trocar) - Primary ID 2015-9621J

Device Regulatory Overview

The Silicone Endo Drain Kit (J Connector+Trocar) (Model/Catalog Number: 2015-9621J) is a medical device manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. This product is indexed under FDA Product Code / Category Classification GCD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2015-9621J
Product Code / EMDN
GCD
Device Name
Database Sync Date
2026-08-09 09:29:18

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 Silicone Endo Drain Kit (J Connector+Trocar)?

The registered manufacturer of record for Silicone Endo Drain Kit (J Connector+Trocar) is FORTUNE MEDICAL INSTRUMENT CORP..

What is the Primary UDI-DI identifier for Silicone Endo Drain Kit (J Connector+Trocar)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2015-9621J.

What classification code is assigned to this device?

This device is registered under product classification code GCD.

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