eudamed_udi
Primary ID: 06973668361025
Centrifuge (UDI 06973668361025)
Manufactured by Jinan Biobase Biotech Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Centrifuge - Primary ID 06973668361025
Device Regulatory Overview
The Centrifuge (Model/Catalog Number: BKC-AU5BT) is a medical device manufactured by Jinan Biobase Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BKC-AU5BT
- Product Code / EMDN
- W02069003
- Device Name
- Centrifuge
- Database Sync Date
- 2026-08-09 16:30:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Centrifuge?
The registered manufacturer of record for Centrifuge is Jinan Biobase Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Centrifuge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973668361025.
What classification code is assigned to this device?
This device is registered under product classification code W02069003.
Similar Classification Devices (W02069003)
Other Devices by Jinan Biobase Biotech Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint