LENTELL IleoBag II S; transparent; clamp (UDI 03858892215517)
Manufactured by Lentismed d.o.o.
Device Regulatory Overview
The LENTELL IleoBag II S; transparent; clamp (Model/Catalog Number: 201110-1C) 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
- 201110-1C
- Product Code / EMDN
- A10020301
- Device Name
- Ostomy Products
- Database Sync Date
- 2026-08-09 16:46:12
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 IleoBag II S; transparent; clamp?
The registered manufacturer of record for LENTELL IleoBag II S; transparent; clamp is Lentismed d.o.o..
What is the Primary UDI-DI identifier for LENTELL IleoBag II S; transparent; clamp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892215517.
What classification code is assigned to this device?
This device is registered under product classification code A10020301.
Similar Classification Devices (A10020301)
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