GUDIDData
eudamed_udi Primary ID: 04048486172374

Osteolind® mobil Miederbody - Mittel - mit BH Cup (UDI 04048486172374)

Manufactured by Werkmeister GmbH + Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Osteolind® mobil Miederbody - Mittel - mit BH Cup - Primary ID 04048486172374

Device Regulatory Overview

The Osteolind® mobil Miederbody - Mittel - mit BH Cup (Model/Catalog Number: 90914) is a medical device manufactured by Werkmeister GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
90914
Product Code / EMDN
Y060309
Device Name
Rumpfstützorthese
Database Sync Date
2026-08-09 16:28:57

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 Osteolind® mobil Miederbody - Mittel - mit BH Cup?

The registered manufacturer of record for Osteolind® mobil Miederbody - Mittel - mit BH Cup is Werkmeister GmbH + Co. KG.

What is the Primary UDI-DI identifier for Osteolind® mobil Miederbody - Mittel - mit BH Cup?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048486172374.

What classification code is assigned to this device?

This device is registered under product classification code Y060309.

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