GUDIDData
eudamed_udi Primary ID: 03858881100916

LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M (UDI 03858881100916)

Manufactured by Lola Ribar d.o.o. za proizvodnju saniteta

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M - Primary ID 03858881100916

Device Regulatory Overview

The LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M (Model/Catalog Number: 1835L) is a medical device manufactured by Lola Ribar d.o.o. za proizvodnju saniteta. This product is indexed under FDA Product Code / Category Classification M0304010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1835L
Product Code / EMDN
M0304010103
Device Name
Nesterilni medicinski proizvodi/ Non sterile medical device
Database Sync Date
2026-08-09 16:51:30

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 LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M?

The registered manufacturer of record for LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M is Lola Ribar d.o.o. za proizvodnju saniteta.

What is the Primary UDI-DI identifier for LOLA CARE LOLIFLEX TKANI ELASTIČNI ZAVOJ 10 CM X 10 M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858881100916.

What classification code is assigned to this device?

This device is registered under product classification code M0304010103.

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