gudid
Primary ID: KNE-X
BMI (UDI KNE-X)
Manufactured by Blake Manufacturing, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BMI - Primary ID KNE-X
Device Regulatory Overview
The BMI (Model/Catalog Number: KNE-X) is a medical device manufactured by Blake Manufacturing, Inc.. This product is indexed under FDA Product Code / Category Classification ITQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KNE-X
- Product Code / EMDN
- ITQ
- Device Name
- Knee, Neoprene Orthosis, size Extra-Large
- Database Sync Date
- 2026-08-09 09:04:02
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 BMI?
The registered manufacturer of record for BMI is Blake Manufacturing, Inc..
What is the Primary UDI-DI identifier for BMI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KNE-X.
What classification code is assigned to this device?
This device is registered under product classification code ITQ.
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