gudid
Primary ID: 4522-A
Bucket (UDI 4522-A)
Manufactured by Andreas Hettich GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bucket - Primary ID 4522-A
Device Regulatory Overview
The Bucket (Model/Catalog Number: 4522-A) is a medical device manufactured by Andreas Hettich GmbH. This product is indexed under FDA Product Code / Category Classification KSO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4522-A
- Product Code / EMDN
- KSO
- Device Name
- Centrifuge Bucket / Tube Holder A device intended to compensate for and enable the use of different size test tubes and bottles in a centrifuge rotor bucket or centrifuge tube holder. This is a reusable device.
- Database Sync Date
- 2026-08-09 09:26:15
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 Bucket?
The registered manufacturer of record for Bucket is Andreas Hettich GmbH.
What is the Primary UDI-DI identifier for Bucket?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4522-A.
What classification code is assigned to this device?
This device is registered under product classification code KSO.
Similar Classification Devices (KSO)
Other Devices by Andreas Hettich GmbH
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