eudamed_udi
Primary ID: 03858892215210
LENTELL IleoTouch S (UDI 03858892215210)
Manufactured by Lentismed d.o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LENTELL IleoTouch S - Primary ID 03858892215210
Device Regulatory Overview
The LENTELL IleoTouch S (Model/Catalog Number: 201107C) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A1001020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201107C
- Product Code / EMDN
- A1001020102
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 17:07:52
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 LENTELL IleoTouch S?
The registered manufacturer of record for LENTELL IleoTouch S is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL IleoTouch S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892215210.
What classification code is assigned to this device?
This device is registered under product classification code A1001020102.
Similar Classification Devices (A1001020102)
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