GUDIDData
eudamed_udi Primary ID: 03858892212158

CompactCath Tiemann, Male, 18 Fr/Ch, 40cm (UDI 03858892212158)

Manufactured by Lentismed d.o.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CompactCath Tiemann, Male, 18 Fr/Ch, 40cm - Primary ID 03858892212158

Device Regulatory Overview

The CompactCath Tiemann, Male, 18 Fr/Ch, 40cm (Model/Catalog Number: 101624) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification U01010601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
101624
Product Code / EMDN
U01010601
Device Name
Pre-lubricated urinary catheter
Database Sync Date
2026-08-09 16:51:41

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of CompactCath Tiemann, Male, 18 Fr/Ch, 40cm?

The registered manufacturer of record for CompactCath Tiemann, Male, 18 Fr/Ch, 40cm is Lentismed d.o.o..

What is the Primary UDI-DI identifier for CompactCath Tiemann, Male, 18 Fr/Ch, 40cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892212158.

What classification code is assigned to this device?

This device is registered under product classification code U01010601.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint