eudamed_udi
Primary ID: 08936206201250
Unspecified Brand (UDI 08936206201250)
Manufactured by Hong Ky Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08936206201250
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 9552) is a medical device manufactured by Hong Ky Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9552
- Product Code / EMDN
- V080602
- Device Name
- Manual Bed
- Database Sync Date
- 2026-08-09 16:29:32
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Hong Ky Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08936206201250.
What classification code is assigned to this device?
This device is registered under product classification code V080602.
Similar Classification Devices (V080602)
Other Devices by Hong Ky Co., Ltd.
Programmatic Export
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