eudamed_udi
Primary ID: 03858892210918
LentisCath Tiemann, Male, 10 Fr/Ch, 40cm (UDI 03858892210918)
Manufactured by Lentismed d.o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LentisCath Tiemann, Male, 10 Fr/Ch, 40cm - Primary ID 03858892210918
Device Regulatory Overview
The LentisCath Tiemann, Male, 10 Fr/Ch, 40cm (Model/Catalog Number: 101420) 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
- 101420
- Product Code / EMDN
- U01010601
- 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 LentisCath Tiemann, Male, 10 Fr/Ch, 40cm?
The registered manufacturer of record for LentisCath Tiemann, Male, 10 Fr/Ch, 40cm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LentisCath Tiemann, Male, 10 Fr/Ch, 40cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892210918.
What classification code is assigned to this device?
This device is registered under product classification code U01010601.
Similar Classification Devices (U01010601)
Other Devices by Lentismed d.o.o.
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