eudamed_udi
Primary ID: 03858892210154
Lenty Nelaton, Female, 16 Fr/Ch, 19cm (UDI 03858892210154)
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 Nelaton, Female, 16 Fr/Ch, 19cm - Primary ID 03858892210154
Device Regulatory Overview
The Lenty Nelaton, Female, 16 Fr/Ch, 19cm (Model/Catalog Number: 101310) 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
- 101310
- Product Code / EMDN
- U01010501
- Device Name
- Intermittent Urinary Catheter
- Database Sync Date
- 2026-08-09 16:29:07
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 Lenty Nelaton, Female, 16 Fr/Ch, 19cm?
The registered manufacturer of record for Lenty Nelaton, Female, 16 Fr/Ch, 19cm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for Lenty Nelaton, Female, 16 Fr/Ch, 19cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892210154.
What classification code is assigned to this device?
This device is registered under product classification code U01010501.
Similar Classification Devices (U01010501)
Other Devices by Lentismed d.o.o.
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