Akicare JSM-055 Reusable Biopsy Needle Guide for Fujifilm UST-9133 / C22K

This catalogue record covers the Akicare JSM-055 Reusable Biopsy Needle Guide, a part reference matched to Fujifilm UST-9133 and C22K probes. The product type is a reusable biopsy needle guide, and the catalogue title confirms its intended use as a needle guide and biopsy adaptor for those Fujifilm Healthcare probe references.

Procurement teams should treat this record as a starting point for compatibility mapping across the listed host systems. Because the guide configuration, probe label details and requested puncture approach each affect fit, the technical match must be confirmed against the physical probe before ordering. Commercial arrangements are separate: packaging, freight, lead time and test scope for this guide are agreed case by case after direct contact, and no timeline or term is promised in this catalogue.

For a similar reusable needle guide, see the related listing under Biopsy Guides: Akicare JSM-054 Reusable Biopsy Needle Guide for Fujifilm EUP-L75 / L64 / UST-5417.

Frequently asked questions

What should I ask about shipping and packaging for the JSM-055 when I contact your team?

Request the exact packaging dimensions, whether the guide ships in a protective tray or pouch, and the freight method for your destination. Also ask about export documentation and any minimum order quantity for this reference. These terms are finalised against the specific order, not fixed in the catalogue.

Specific to this model, how do I verify the probe connector and label match before I request a quote?

Photograph the full probe model label, including the connector type and serial number. Confirm that the probe reads UST-9133 or C22K exactly. Then state the guide reference JSM-055 and ask whether the mounting bracket aligns with your probe’s connector housing.

Which details must I include in my enquiry to get a useful response about this guide?

Send your probe model and serial number, the exact guide reference, the needle gauge and puncture approach, and the intended procedure. Also specify the required sterile or non-sterile packaging and any disinfection method. The team will then confirm compatibility and commercial terms for that specific request.