gudid
Primary ID: 60-640-240
KaWe (UDI 60-640-240)
Manufactured by BV Medical
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KaWe - Primary ID 60-640-240
Device Regulatory Overview
The KaWe (Model/Catalog Number: 60-640-240) is a medical device manufactured by BV Medical. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60-640-240
- Product Code / EMDN
- KYT
- Device Name
- KaWe Cliplight Diagnostic Penlight, Red
- Database Sync Date
- 2026-08-09 09:21:02
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 KaWe?
The registered manufacturer of record for KaWe is BV Medical.
What is the Primary UDI-DI identifier for KaWe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60-640-240.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
Other Devices by BV Medical
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