eudamed_udi
Primary ID: 04260531792577
V-TIP (UDI 04260531792577)
Manufactured by VITROMED GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V-TIP - Primary ID 04260531792577
Device Regulatory Overview
The V-TIP (Model/Catalog Number: V-TIP-1000) is a medical device manufactured by VITROMED GmbH. This product is indexed under FDA Product Code / Category Classification W0503020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V-TIP-1000
- Product Code / EMDN
- W0503020202
- Device Name
- V-TIP
- Database Sync Date
- 2026-08-09 16:49:16
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 V-TIP?
The registered manufacturer of record for V-TIP is VITROMED GmbH.
What is the Primary UDI-DI identifier for V-TIP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260531792577.
What classification code is assigned to this device?
This device is registered under product classification code W0503020202.
Similar Classification Devices (W0503020202)
Other Devices by VITROMED GmbH
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