eudamed_udi
Primary ID: 03858892214497
LENTELL OstoZip II (UDI 03858892214497)
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 OstoZip II - Primary ID 03858892214497
Device Regulatory Overview
The LENTELL OstoZip II (Model/Catalog Number: 201126) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A100205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201126
- Product Code / EMDN
- A100205
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:28:56
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 OstoZip II?
The registered manufacturer of record for LENTELL OstoZip II is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL OstoZip II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892214497.
What classification code is assigned to this device?
This device is registered under product classification code A100205.
Similar Classification Devices (A100205)
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