gudid
Primary ID: 30087532 01
HYDROFLEX ELISA (UDI 30087532 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 ELISA - Primary ID 30087532 01
Device Regulatory Overview
The HYDROFLEX ELISA (Model/Catalog Number: 30087532 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
- 30087532 01
- Product Code / EMDN
- LXG
- Device Name
- Microplate washer
- Database Sync Date
- 2026-08-09 09:29:32
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 HYDROFLEX ELISA?
The registered manufacturer of record for HYDROFLEX ELISA is Tecan Austria GmbH.
What is the Primary UDI-DI identifier for HYDROFLEX ELISA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30087532 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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint