eudamed_udi
Primary ID: 03858892217863
LENTELL IleoBag II XXS; transparent (UDI 03858892217863)
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 XXS; transparent - Primary ID 03858892217863
Device Regulatory Overview
The LENTELL IleoBag II XXS; transparent (Model/Catalog Number: 201165-1) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A10020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201165-1
- Product Code / EMDN
- A10020301
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:44:49
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LENTELL IleoBag II XXS; transparent?
The registered manufacturer of record for LENTELL IleoBag II XXS; transparent is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL IleoBag II XXS; transparent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892217863.
What classification code is assigned to this device?
This device is registered under product classification code A10020301.
Similar Classification Devices (A10020301)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint