eudamed_udi Primary ID: 08435491805841

ARNES POST-QUIRURGICO SEÑORA T.L M: 100-115 ; WOMEN’S CHEST HARNESS (UDI 08435491805841)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ARNES POST-QUIRURGICO SEÑORA T.L M: 100-115 ; WOMEN’S CHEST HARNESS (Model/Catalog Number: 1302#L) 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#L
Product Code / EMDN: Y180999
Device Name: Arneses
Database Sync Date: 2026-08-09 16:44:57

Full Regulatory Attributes

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{
    "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.L M: 100-115 ; WOMEN’S CHEST HARNESS?

The registered manufacturer of record for ARNES POST-QUIRURGICO SEÑORA T.L M: 100-115 ; WOMEN’S CHEST HARNESS is Orliman, S.L.U..

What is the Primary UDI-DI identifier for ARNES POST-QUIRURGICO SEÑORA T.L M: 100-115 ; WOMEN’S CHEST HARNESS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435491805841.

What classification code is assigned to this device?

This device is registered under product classification code Y180999.

Similar Classification Devices (Y180999)

Other Devices by Orliman, S.L.U.

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