eudamed_udi
Primary ID: 06931038600495
CUFF (UDI 06931038600495)
Manufactured by Wenzhou Bokang Instruments Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUFF - Primary ID 06931038600495
Device Regulatory Overview
The CUFF (Model/Catalog Number: 026+056.1) is a medical device manufactured by Wenzhou Bokang Instruments Co.,Ltd. This product is indexed under FDA Product Code / Category Classification R01038001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 026+056.1
- Product Code / EMDN
- R01038001
- Device Name
- blood pressure cuff
- Database Sync Date
- 2026-08-09 18:37:02
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 CUFF?
The registered manufacturer of record for CUFF is Wenzhou Bokang Instruments Co.,Ltd.
What is the Primary UDI-DI identifier for CUFF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931038600495.
What classification code is assigned to this device?
This device is registered under product classification code R01038001.
Similar Classification Devices (R01038001)
Other Devices by Wenzhou Bokang Instruments Co.,Ltd
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