GUDIDData
gudid Primary ID: 000000014049559088

ASP6025 S China (UDI 000000014049559088)

Manufactured by Leica Biosystems Nussloch GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASP6025 S China - Primary ID 000000014049559088

Device Regulatory Overview

The ASP6025 S China (Model/Catalog Number: 000000014049559088) is a medical device manufactured by Leica Biosystems Nussloch GmbH. This product is indexed under FDA Product Code / Category Classification IEO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
000000014049559088
Product Code / EMDN
IEO
Device Name
The ASP6025 S Tissue Processor is a modular tissue processor for the following laboratory applications: Fixation Dehydration Infiltration with intermedium Paraffin infiltration of histological tissue specimens. The ASP6025 S can be used as medical IVD product. The improved features of the ASP6025 S are the combination of: Reduced processing time Easier reagent exchange Monitoring the ethanol quality by density measurement as well as the Ability to replace xylene, a substance that is hazardous (including to the health), with special process protocols. The instrument has been designed so that it is safe to use by the operator as well as for processing specimens. However, the prerequisite for this is that it is operated according to these Instructions for Use.
Database Sync Date
2026-08-09 09:11:27

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 ASP6025 S China?

The registered manufacturer of record for ASP6025 S China is Leica Biosystems Nussloch GmbH.

What is the Primary UDI-DI identifier for ASP6025 S China?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000000014049559088.

What classification code is assigned to this device?

This device is registered under product classification code IEO.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint