Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003992063

FEI Number

3003992063

Entity Name

Brooks Laboratory Automation Solutions PTY LTD

City/State/Country

VIRGINIA, Queensland, AU

Establishment Address

15 Lisgar Street, VIRGINIA, Queensland 4014, AU

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Aim Lab Automation Technologies Pty Ltd (Owner Number: 9071560)

Owner / Operator Contact Address

15 Lisgar Street, --, Virginia, AU-QLD 4014, AU

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PathFinder 350D Plus Decapper Double Sorter PathFinder 450S Sorter PathFinder 350D Decapper Sorter PathFinder 350A Archiver

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2005-03-22

Official Correspondent

NICK LASZLO

US Agent Details

Jessica Wenzell Business: Brooks Automation US, LLC Email: jessica.wenzell@brooksautomation.com Phone: (717) 2509599

Related Public Records

Same Entity

Aim Lab Automation Technologies Pty Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003992063. Last updated year: 2026. Please use registration number 3003992063 when referencing this establishment in official correspondence.