eudamed_udi
Primary ID: 03858892211120
LENTELL ColoBag II XS (UDI 03858892211120)
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 XS - Primary ID 03858892211120
Device Regulatory Overview
The LENTELL ColoBag II XS (Model/Catalog Number: 201138) is a medical device manufactured by Lentismed d.o.o.. This product is indexed under FDA Product Code / Category Classification A10020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 201138
- Product Code / EMDN
- A10020201
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:49:47
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 XS?
The registered manufacturer of record for LENTELL ColoBag II XS is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL ColoBag II XS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892211120.
What classification code is assigned to this device?
This device is registered under product classification code A10020201.
Similar Classification Devices (A10020201)
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