GUDIDData
eudamed_udi Primary ID: 08435025959743

BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION (UDI 08435025959743)

Manufactured by Orliman, S.L.U.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION - Primary ID 08435025959743

Device Regulatory Overview

The BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION (Model/Catalog Number: BOD-100T#120) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BOD-100T#120
Product Code / EMDN
Y060309
Device Name
O.T Elástica (Bodys)
Database Sync Date
2026-08-09 16:29:16

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 BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION?

The registered manufacturer of record for BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION is Orliman, S.L.U..

What is the Primary UDI-DI identifier for BODY BODYOSTEC CON TRACCION T.120 M: 116-120 ; BODY FOR OSTEOPOROSIS WITH TRACTION?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435025959743.

What classification code is assigned to this device?

This device is registered under product classification code Y060309.

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