GUDIDData
eudamed_udi Primary ID: 09551004191467

SERIX NAVY (UDI 09551004191467)

Manufactured by TG MEDICAL SDN. BHD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SERIX NAVY - Primary ID 09551004191467

Device Regulatory Overview

The SERIX NAVY (Model/Catalog Number: MED-100419006) is a medical device manufactured by TG MEDICAL SDN. BHD.. This product is indexed under FDA Product Code / Category Classification T01020204 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MED-100419006
Product Code / EMDN
T01020204
Device Name
Nitrile Examination Powder Free Gloves
Database Sync Date
2026-08-09 16:48:44

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 SERIX NAVY?

The registered manufacturer of record for SERIX NAVY is TG MEDICAL SDN. BHD..

What is the Primary UDI-DI identifier for SERIX NAVY?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09551004191467.

What classification code is assigned to this device?

This device is registered under product classification code T01020204.

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