LentisCath+ Nelaton, Female, 10 Fr/Ch, 19cm (UDI 03858892211328)
Manufactured by Lentismed d.o.o.
Device Regulatory Overview
The LentisCath+ Nelaton, Female, 10 Fr/Ch, 19cm (Model/Catalog Number: 101507) 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
- 101507
- Product Code / EMDN
- U01010501
- Device Name
- Intermittent Urinary Catheter
- Database Sync Date
- 2026-08-09 17:06:56
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LentisCath+ Nelaton, Female, 10 Fr/Ch, 19cm?
The registered manufacturer of record for LentisCath+ Nelaton, Female, 10 Fr/Ch, 19cm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LentisCath+ Nelaton, Female, 10 Fr/Ch, 19cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892211328.
What classification code is assigned to this device?
This device is registered under product classification code U01010501.
Similar Classification Devices (U01010501)
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