LentisCath Nelaton, Female, 14 Fr/Ch, 20cm (UDI 03858892210741)
Manufactured by Lentismed d.o.o.
Device Regulatory Overview
The LentisCath Nelaton, Female, 14 Fr/Ch, 20cm (Model/Catalog Number: 101409) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification U01010501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101409
- Product Code / EMDN
- U01010501
- Device Name
- Intermittent Urinary Catheter
- Database Sync Date
- 2026-08-09 16:50:58
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 LentisCath Nelaton, Female, 14 Fr/Ch, 20cm?
The registered manufacturer of record for LentisCath Nelaton, Female, 14 Fr/Ch, 20cm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LentisCath Nelaton, Female, 14 Fr/Ch, 20cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892210741.
What classification code is assigned to this device?
This device is registered under product classification code U01010501.
Similar Classification Devices (U01010501)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint