eudamed_udi
Primary ID: 08809317171418
MEDINAUT-V (UDI 08809317171418)
Manufactured by IMEDICOM Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDINAUT-V - Primary ID 08809317171418
Device Regulatory Overview
The MEDINAUT-V (Model/Catalog Number: H-CAT-004-US-01) is a medical device manufactured by IMEDICOM Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H-CAT-004-US-01
- Product Code / EMDN
- K010302
- Device Name
- Vertebral Augmentation System
- Database Sync Date
- 2026-08-09 16:30:26
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 MEDINAUT-V?
The registered manufacturer of record for MEDINAUT-V is IMEDICOM Co., Ltd..
What is the Primary UDI-DI identifier for MEDINAUT-V?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809317171418.
What classification code is assigned to this device?
This device is registered under product classification code K010302.
Similar Classification Devices (K010302)
Other Devices by IMEDICOM Co., Ltd.
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