eudamed_udi
Primary ID: 08809295147368
V-TIP (UDI 08809295147368)
Manufactured by RF Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V-TIP - Primary ID 08809295147368
Device Regulatory Overview
The V-TIP (Model/Catalog Number: VCTW 30XXB) is a medical device manufactured by RF Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VCTW 30XXB
- Product Code / EMDN
- K0201010301
- Device Name
- V-TIP, MYOBLATE-V™, OsteoBlate™, VertiBlate™
- Database Sync Date
- 2026-08-09 16:30:33
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 RF Medical Co., Ltd..
What is the Primary UDI-DI identifier for V-TIP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809295147368.
What classification code is assigned to this device?
This device is registered under product classification code K0201010301.
Similar Classification Devices (K0201010301)
Other Devices by RF Medical Co., Ltd.
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