eudamed_udi
Primary ID: 03858892214077
LENTELL ColoBag II L (UDI 03858892214077)
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 ColoBag II L - Primary ID 03858892214077
Device Regulatory Overview
The LENTELL ColoBag II L (Model/Catalog Number: 201105) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A10020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201105
- Product Code / EMDN
- A10020202
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 17:05:52
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 ColoBag II L?
The registered manufacturer of record for LENTELL ColoBag II L is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL ColoBag II L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892214077.
What classification code is assigned to this device?
This device is registered under product classification code A10020202.
Similar Classification Devices (A10020202)
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