GUDIDData
eudamed_udi Primary ID: 08435491805834

ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS (UDI 08435491805834)

Manufactured by Orliman, S.L.U.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS - Primary ID 08435491805834

Device Regulatory Overview

The ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS (Model/Catalog Number: 1302#M) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y180999 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1302#M
Product Code / EMDN
Y180999
Device Name
Arneses
Database Sync Date
2026-08-09 16:29:38

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 ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS?

The registered manufacturer of record for ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS is Orliman, S.L.U..

What is the Primary UDI-DI identifier for ARNES POST-QUIRURGICO SEÑORA T.M M: 85-100 ; WOMEN’S CHEST HARNESS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435491805834.

What classification code is assigned to this device?

This device is registered under product classification code Y180999.

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