Identity
- Trade Name
- PATHFINDER FDA UDI
- Generic Name
- Specimen processing instrument IVD FDA UDI
- Device Name
- PATHFINDER 900 PLUS DCS AUTOMATED TUBE MANAGEMENT SYSTEM FOR DECAPPING, CAPPING AND SORTING, SET UP FOR 20 INPUT/OUTPUT POSITIONS FDA UDI
- Model / Reference
- PS-U-A1205 FDA UDI
- Description
- PATHFINDER 900 PLUS DCS AUTOMATED TUBE MANAGEMENT SYSTEM FOR DECAPPING, CAPPING AND SORTING, SET UP FOR 20 INPUT/OUTPUT POSITIONS FDA UDI
Identifiers
- Catalog Number
- 06R6105 FDA UDI
- Primary DI / UDI-DI
- 09356119001041 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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aim Lab Automation Technologies Pty Ltd
Sources (1)
- FDA UDI b245f7bc-27e3-4e89-bea2-c23111d8593b 36 fields · synced Jun 6, 2026