gudid
Primary ID: 55-95003-401
VQ ORTHOCARE (UDI 55-95003-401)
Manufactured by Vision Quest Industries Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VQ ORTHOCARE - Primary ID 55-95003-401
Device Regulatory Overview
The VQ ORTHOCARE (Model/Catalog Number: 55-95003-401) is a medical device manufactured by Vision Quest Industries Incorporated. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 55-95003-401
- Product Code / EMDN
- NYN
- Device Name
- BIONICARE KNEE SYSTEM LEFT 2XL/3XL
- Database Sync Date
- 2026-08-09 09:32:58
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 VQ ORTHOCARE?
The registered manufacturer of record for VQ ORTHOCARE is Vision Quest Industries Incorporated.
What is the Primary UDI-DI identifier for VQ ORTHOCARE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 55-95003-401.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by Vision Quest Industries Incorporated
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