GUDIDData
eudamed_udi Primary ID: 00806363506056

Gant d’intervention chirurgicale SP Bord roulé (UDI 00806363506056)

Manufactured by Kanam Latex Industries Private Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gant d’intervention chirurgicale SP Bord roulé - Primary ID 00806363506056

Device Regulatory Overview

The Gant d’intervention chirurgicale SP Bord roulé (Model/Catalog Number: 114204P) is a medical device manufactured by Kanam Latex Industries Private Limited. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
114204P
Product Code / EMDN
T01010102
Device Name
Sterile Latex Surgical Gloves Powder Free
Database Sync Date
2026-08-09 16:29:59

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 Gant d’intervention chirurgicale SP Bord roulé?

The registered manufacturer of record for Gant d’intervention chirurgicale SP Bord roulé is Kanam Latex Industries Private Limited.

What is the Primary UDI-DI identifier for Gant d’intervention chirurgicale SP Bord roulé?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00806363506056.

What classification code is assigned to this device?

This device is registered under product classification code T01010102.

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