<?xml version='1.0' encoding='UTF-8'?><device xmlns='http://www.fda.gov/cdrh/gudid' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance'><publicDeviceRecordKey>f7016374-fe06-41c1-b7b8-624074b6e6ab</publicDeviceRecordKey><publicVersionStatus>New</publicVersionStatus><deviceRecordStatus>Published</deviceRecordStatus><publicVersionNumber>1</publicVersionNumber><publicVersionDate>2026-04-02</publicVersionDate><devicePublishDate>2026-03-25</devicePublishDate><deviceCommDistributionEndDate xsi:nil="true"/><deviceCommDistributionStatus>In Commercial Distribution</deviceCommDistributionStatus><identifiers><identifier><deviceId>B040RPS18500</deviceId><deviceIdType>Primary</deviceIdType><deviceIdIssuingAgency>HIBCC</deviceIdIssuingAgency><containsDINumber xsi:nil="true"/><pkgQuantity xsi:nil="true"/><pkgDiscontinueDate xsi:nil="true"/><pkgStatus xsi:nil="true"/><pkgType xsi:nil="true"/></identifier></identifiers><brandName>Thoracic Port with Obturator 18x50mm</brandName><versionModelNumber>RPS-1850</versionModelNumber><catalogNumber xsi:nil="true"/><dunsNumber>939872651</dunsNumber><companyName>GENESEE BIOMEDICAL, INC.</companyName><deviceCount>1</deviceCount><deviceDescription>Thoracic Port with Obturator 18 mm ID x 50 mm Length
</deviceDescription><DMExempt>false</DMExempt><premarketExempt>true</premarketExempt><deviceHCTP>false</deviceHCTP><deviceKit>false</deviceKit><deviceCombinationProduct>false</deviceCombinationProduct><singleUse>false</singleUse><lotBatch>true</lotBatch><serialNumber>false</serialNumber><manufacturingDate>true</manufacturingDate><expirationDate>false</expirationDate><donationIdNumber>false</donationIdNumber><labeledContainsNRL>false</labeledContainsNRL><labeledNoNRL>false</labeledNoNRL><MRISafetyStatus>Labeling does not contain MRI Safety Information</MRISafetyStatus><rx>true</rx><otc>false</otc><contacts><customerContact><phone>1-800-786-4880</phone><phoneExtension xsi:nil="true"/><email>cservice@geneseebiomedical.com</email></customerContact></contacts><gmdnTerms><gmdn><gmdnCode>62857</gmdnCode><gmdnPTName>Pleuroscopic/mediastinoscopic access cannula, reusable</gmdnPTName><gmdnPTDefinition>A rigid, single-lumen, surgical instrument intended to be percutaneously inserted through the chest to provide access to the pleural and/or mediastinal cavity to facilitate the introduction of surgical instruments as part of a minimally-invasive procedure; it is not intended for pericardial access. It provides an entry between adjacent ribs and once in place is intended to remain in position for the duration of the procedure. It may include a trocar with a sharp or blunt tip intended to assist introduction; devices with the trocar included it may be referred to as a trocar or trocar assembly. This is a reusable device.</gmdnPTDefinition><implantable>false</implantable><gmdnCodeStatus>Active</gmdnCodeStatus></gmdn></gmdnTerms><productCodes><fdaProductCode><productCode>DWS</productCode><productCodeName>Instruments, Surgical, Cardiovascular</productCodeName></fdaProductCode></productCodes><deviceSizes/><environmentalConditions/><sterilization><deviceSterile>false</deviceSterile><sterilizationPriorToUse>true</sterilizationPriorToUse><methodTypes><sterilizationMethod>Moist Heat or Steam Sterilization</sterilizationMethod></methodTypes></sterilization></device>