GUDIDData
eudamed_udi Primary ID: 08029513126474

IPER Lady Light Mini (UDI 08029513126474)

Manufactured by Santex S.p.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IPER Lady Light Mini - Primary ID 08029513126474

Device Regulatory Overview

The IPER Lady Light Mini (Model/Catalog Number: W31SL10BD-20B) is a medical device manufactured by Santex S.p.A.. This product is indexed under FDA Product Code / Category Classification T04010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
W31SL10BD-20B
Product Code / EMDN
T04010102
Device Name
Pannoloni sagomati donna per piccola incontinenza
Database Sync Date
2026-08-09 16:45:58

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 IPER Lady Light Mini?

The registered manufacturer of record for IPER Lady Light Mini is Santex S.p.A..

What is the Primary UDI-DI identifier for IPER Lady Light Mini?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08029513126474.

What classification code is assigned to this device?

This device is registered under product classification code T04010102.

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