eudamed_udi
Primary ID: 08049033192308
EXTENSION LINE (UDI 08049033192308)
Manufactured by Know Medical Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXTENSION LINE - Primary ID 08049033192308
Device Regulatory Overview
The EXTENSION LINE (Model/Catalog Number: EL100005-O) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EL100005-O
- Product Code / EMDN
- A03020101
- Device Name
- EXTENSION LINE - Prolunga 3x4,1 50cm LLM-LLF
- Database Sync Date
- 2026-08-09 16:29:10
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 EXTENSION LINE?
The registered manufacturer of record for EXTENSION LINE is Know Medical Srl.
What is the Primary UDI-DI identifier for EXTENSION LINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08049033192308.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
Other Devices by Know Medical Srl
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