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Pathfinder

FDA UDI

Class I (US FDA UDI)

by Aim Lab Automation Technologies Pty Ltd

Identity

Trade Name
PATHFINDER FDA UDI
Generic Name
Specimen processing instrument IVD FDA UDI
Device Name
PATHFINDER 350A ARCHIVER FOR ABBOTT ARCHITECT RACK FDA UDI
Model / Reference
PS-U-A084 FDA UDI
Description
PATHFINDER 350A ARCHIVER FOR ABBOTT ARCHITECT RACK FDA UDI

Identifiers

Catalog Number
04Z7303 FDA UDI
Primary DI / UDI-DI
09356119002222 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Specimen processing instrument IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen processing instrument IVD

Pathfinder by Aim Lab Automation Technologies Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen processing instrument IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 879c62b7-5c2d-47b3-9adf-2c68ca453071 36 fields · synced May 31, 2026