GUDIDData
eudamed_udi Primary ID: 04046963817237

Vasco Nitril light (UDI 04046963817237)

Manufactured by HARPS Investment Asia Pte. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vasco Nitril light - Primary ID 04046963817237

Device Regulatory Overview

The Vasco Nitril light (Model/Catalog Number: 9207732) is a medical device manufactured by HARPS Investment Asia Pte. Ltd.. This product is indexed under FDA Product Code / Category Classification T01020204 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9207732
Product Code / EMDN
T01020204
Device Name
Non sterile, single use, powder free, nitrile, examination glove, ambidextrous, violet blue
Database Sync Date
2026-08-09 16:28:55

Full Regulatory Attributes

πŸ”’ 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 Vasco Nitril light?

The registered manufacturer of record for Vasco Nitril light is HARPS Investment Asia Pte. Ltd..

What is the Primary UDI-DI identifier for Vasco Nitril light?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046963817237.

What classification code is assigned to this device?

This device is registered under product classification code T01020204.

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