eudamed_udi
Primary ID: 03858892215357
LENTELL IleoBag II Kids (UDI 03858892215357)
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 IleoBag II Kids - Primary ID 03858892215357
Device Regulatory Overview
The LENTELL IleoBag II Kids (Model/Catalog Number: 201112F) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A10020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201112F
- Product Code / EMDN
- A10020302
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:50:58
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 IleoBag II Kids?
The registered manufacturer of record for LENTELL IleoBag II Kids is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL IleoBag II Kids?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892215357.
What classification code is assigned to this device?
This device is registered under product classification code A10020302.
Similar Classification Devices (A10020302)
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