gudid Primary ID: BIOSPA-SI

BIOSPA-SI (UDI BIOSPA-SI)

Manufactured by AGILENT TECHNOLOGIES, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BIOSPA-SI (Model/Catalog Number: BIOSPA-SI) is a medical device manufactured by AGILENT TECHNOLOGIES, INC.. This product is indexed under FDA Product Code / Category Classification JTQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BIOSPA-SI
Product Code / EMDN: JTQ
Device Name: Automated Incubator
Database Sync Date: 2026-08-09 09:57:21

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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Frequently Asked Questions

Who is the primary manufacturer of BIOSPA-SI?

The registered manufacturer of record for BIOSPA-SI is AGILENT TECHNOLOGIES, INC..

What is the Primary UDI-DI identifier for BIOSPA-SI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BIOSPA-SI.

What classification code is assigned to this device?

This device is registered under product classification code JTQ.

Similar Classification Devices (JTQ)

Other Devices by AGILENT TECHNOLOGIES, INC.

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