eudamed_udi Primary ID: 08435025992511

DESROTADOR TIBIOFEMORAL ; TIBIOFEMORAL DEROTATION STRAPS (UDI 08435025992511)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DESROTADOR TIBIOFEMORAL ; TIBIOFEMORAL DEROTATION STRAPS (Model/Catalog Number: OP1173#E) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y061217 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: OP1173#E
Product Code / EMDN: Y061217
Device Name: Musleras elásticas
Database Sync Date: 2026-08-09 16:48:49

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 DESROTADOR TIBIOFEMORAL ; TIBIOFEMORAL DEROTATION STRAPS?

The registered manufacturer of record for DESROTADOR TIBIOFEMORAL ; TIBIOFEMORAL DEROTATION STRAPS is Orliman, S.L.U..

What is the Primary UDI-DI identifier for DESROTADOR TIBIOFEMORAL ; TIBIOFEMORAL DEROTATION STRAPS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435025992511.

What classification code is assigned to this device?

This device is registered under product classification code Y061217.

Similar Classification Devices (Y061217)

Other Devices by Orliman, S.L.U.

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