eudamed_udi
Primary ID: 08800142924620
VertiBlate™ (UDI 08800142924620)
Manufactured by RF Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VertiBlate™ - Primary ID 08800142924620
Device Regulatory Overview
The VertiBlate™ (Model/Catalog Number: BRT 1830B) 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
- BRT 1830B
- Product Code / EMDN
- K0201010301
- Device Name
- V-TIP, MYOBLATE-V™, OsteoBlate™, VertiBlate™
- Database Sync Date
- 2026-08-09 16:29:00
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 VertiBlate™?
The registered manufacturer of record for VertiBlate™ is RF Medical Co., Ltd..
What is the Primary UDI-DI identifier for VertiBlate™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800142924620.
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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