eudamed_udi
Primary ID: 08902120303455
VEIN-O-LINE (UDI 08902120303455)
Manufactured by Romsons International (Unit II)
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VEIN-O-LINE - Primary ID 08902120303455
Device Regulatory Overview
The VEIN-O-LINE (Model/Catalog Number: GS-3034) is a medical device manufactured by Romsons International (Unit II). This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-3034
- Product Code / EMDN
- A03020101
- Device Name
- Extension Line
- Database Sync Date
- 2026-08-09 16:28:58
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 VEIN-O-LINE?
The registered manufacturer of record for VEIN-O-LINE is Romsons International (Unit II).
What is the Primary UDI-DI identifier for VEIN-O-LINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08902120303455.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
Other Devices by Romsons International (Unit II)
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