gudid
Primary ID: 30087534 01
HYDROFLEX EVOLYZER 16CH (UDI 30087534 01)
Manufactured by Tecan Austria GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HYDROFLEX EVOLYZER 16CH - Primary ID 30087534 01
Device Regulatory Overview
The HYDROFLEX EVOLYZER 16CH (Model/Catalog Number: 30087534 01) is a medical device manufactured by Tecan Austria GmbH. This product is indexed under FDA Product Code / Category Classification LXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30087534 01
- Product Code / EMDN
- LXG
- Device Name
- Microplate washer
- Database Sync Date
- 2026-08-09 09:29:32
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 HYDROFLEX EVOLYZER 16CH?
The registered manufacturer of record for HYDROFLEX EVOLYZER 16CH is Tecan Austria GmbH.
What is the Primary UDI-DI identifier for HYDROFLEX EVOLYZER 16CH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30087534 01.
What classification code is assigned to this device?
This device is registered under product classification code LXG.
Similar Classification Devices (LXG)
Other Devices by Tecan Austria GmbH
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