eudamed_udi
Primary ID: 03858892210543
LENTELL Convex II L / pre-cut 28mm (UDI 03858892210543)
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 Convex II L / pre-cut 28mm - Primary ID 03858892210543
Device Regulatory Overview
The LENTELL Convex II L / pre-cut 28mm (Model/Catalog Number: 201122PC-28) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A1002010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201122PC-28
- Product Code / EMDN
- A1002010402
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:45:42
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 Convex II L / pre-cut 28mm?
The registered manufacturer of record for LENTELL Convex II L / pre-cut 28mm is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL Convex II L / pre-cut 28mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892210543.
What classification code is assigned to this device?
This device is registered under product classification code A1002010402.
Similar Classification Devices (A1002010402)
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