eudamed_udi
Primary ID: 06972337851836
Elution Buffer (UDI 06972337851836)
Manufactured by B&E BIO-TECHNOLOGY CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elution Buffer - Primary ID 06972337851836
Device Regulatory Overview
The Elution Buffer (Model/Catalog Number: 60101) is a medical device manufactured by B&E BIO-TECHNOLOGY CO., LTD.. This product is indexed under FDA Product Code / Category Classification W01010214 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60101
- Product Code / EMDN
- W01010214
- Device Name
- Elution Buffer
- Database Sync Date
- 2026-08-09 17:05:58
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 Elution Buffer?
The registered manufacturer of record for Elution Buffer is B&E BIO-TECHNOLOGY CO., LTD..
What is the Primary UDI-DI identifier for Elution Buffer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972337851836.
What classification code is assigned to this device?
This device is registered under product classification code W01010214.
Similar Classification Devices (W01010214)
Other Devices by B&E BIO-TECHNOLOGY CO., LTD.
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