eudamed_udi
Primary ID: 03858892210352
Lenty Tiemann, Male, 18 Fr/Ch, 40cm (UDI 03858892210352)
Manufactured by Lentismed d.o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lenty Tiemann, Male, 18 Fr/Ch, 40cm - Primary ID 03858892210352
Device Regulatory Overview
The Lenty Tiemann, Male, 18 Fr/Ch, 40cm (Model/Catalog Number: 101324) 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
- 101324
- Product Code / EMDN
- U01010601
- Device Name
- Intermittent Urinary Catheter
- Database Sync Date
- 2026-08-09 16:51:46
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 Lenty Tiemann, Male, 18 Fr/Ch, 40cm?
The registered manufacturer of record for Lenty Tiemann, Male, 18 Fr/Ch, 40cm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for Lenty Tiemann, Male, 18 Fr/Ch, 40cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892210352.
What classification code is assigned to this device?
This device is registered under product classification code U01010601.
Similar Classification Devices (U01010601)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint