gudid
Primary ID: 412
Kneehab XP (UDI 412)
Manufactured by BIO-MEDICAL RESEARCH LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kneehab XP - Primary ID 412
Device Regulatory Overview
The Kneehab XP (Model/Catalog Number: 412) is a medical device manufactured by BIO-MEDICAL RESEARCH LIMITED. This product is indexed under FDA Product Code / Category Classification NYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 412
- Product Code / EMDN
- NYN
- Device Name
- Database Sync Date
- 2026-08-09 09:22:51
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 Kneehab XP?
The registered manufacturer of record for Kneehab XP is BIO-MEDICAL RESEARCH LIMITED.
What is the Primary UDI-DI identifier for Kneehab XP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 412.
What classification code is assigned to this device?
This device is registered under product classification code NYN.
Similar Classification Devices (NYN)
Other Devices by BIO-MEDICAL RESEARCH LIMITED
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