GUDIDData
eudamed_udi Primary ID: 05900516697129

SENI AIR CLASSIC (UDI 05900516697129)

Manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SENI AIR CLASSIC - Primary ID 05900516697129

Device Regulatory Overview

The SENI AIR CLASSIC (Model/Catalog Number: SE-094-XL10-ICB) is a medical device manufactured by TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification T04010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SE-094-XL10-ICB
Product Code / EMDN
T04010103
Device Name
ALL-IN-ONE ADULT DIAPERS
Database Sync Date
2026-08-09 16:29:25

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 SENI AIR CLASSIC?

The registered manufacturer of record for SENI AIR CLASSIC is TORUŃSKIE ZAKŁADY MATERIAŁÓW OPATRUNKOWYCH SPÓŁKA AKCYJNA.

What is the Primary UDI-DI identifier for SENI AIR CLASSIC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05900516697129.

What classification code is assigned to this device?

This device is registered under product classification code T04010103.

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