eudamed_udi
Primary ID: 06931038631024
Teqler (UDI 06931038631024)
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 Teqler - Primary ID 06931038631024
Device Regulatory Overview
The Teqler (Model/Catalog Number: T401126) is a medical device manufactured by Wenzhou Bokang Instruments Co.,Ltd. This product is indexed under FDA Product Code / Category Classification C9005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T401126
- Product Code / EMDN
- C9005
- Device Name
- stethoscope
- Database Sync Date
- 2026-08-09 18:07:46
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 Teqler?
The registered manufacturer of record for Teqler is Wenzhou Bokang Instruments Co.,Ltd.
What is the Primary UDI-DI identifier for Teqler?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931038631024.
What classification code is assigned to this device?
This device is registered under product classification code C9005.
Similar Classification Devices (C9005)
Other Devices by Wenzhou Bokang Instruments Co.,Ltd
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