eudamed_udi
Primary ID: D-EL104215-OZN
EXTENSION LINE (UDI D-EL104215-OZN)
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 D-EL104215-OZN
Device Regulatory Overview
The EXTENSION LINE (Model/Catalog Number: EL104215-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
- EL104215-O
- Product Code / EMDN
- A03020101
- Device Name
- EXTENSION LINE - Prolunga 3x4,1 150 cm PVC LLM-LLM
- Database Sync Date
- 2026-08-09 16:58:53
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 D-EL104215-OZN.
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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