eudamed_udi
Primary ID: 06975488440485
Orbital Shaker (UDI 06975488440485)
Manufactured by Infitek Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Orbital Shaker - Primary ID 06975488440485
Device Regulatory Overview
The Orbital Shaker (Model/Catalog Number: SHK-O210) is a medical device manufactured by Infitek Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W02070401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SHK-O210
- Product Code / EMDN
- W02070401
- Device Name
- Shaker
- Database Sync Date
- 2026-08-09 17:47:47
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 Orbital Shaker?
The registered manufacturer of record for Orbital Shaker is Infitek Co., Ltd..
What is the Primary UDI-DI identifier for Orbital Shaker?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975488440485.
What classification code is assigned to this device?
This device is registered under product classification code W02070401.
Similar Classification Devices (W02070401)
Other Devices by Infitek Co., Ltd.
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