<?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>d70b72e8-10ad-4e02-ab86-76ecd031341c</publicDeviceRecordKey><publicVersionStatus>Update</publicVersionStatus><deviceRecordStatus>Published</deviceRecordStatus><publicVersionNumber>5</publicVersionNumber><publicVersionDate>2025-04-16</publicVersionDate><devicePublishDate>2016-09-06</devicePublishDate><deviceCommDistributionEndDate>2025-04-15</deviceCommDistributionEndDate><deviceCommDistributionStatus>Not in Commercial Distribution</deviceCommDistributionStatus><identifiers><identifier><deviceId>08437014205183</deviceId><deviceIdType>Primary</deviceIdType><deviceIdIssuingAgency>GS1</deviceIdIssuingAgency><containsDINumber xsi:nil="true"/><pkgQuantity xsi:nil="true"/><pkgDiscontinueDate xsi:nil="true"/><pkgStatus xsi:nil="true"/><pkgType xsi:nil="true"/></identifier></identifiers><brandName>WADiana Compact</brandName><versionModelNumber>213789</versionModelNumber><catalogNumber>213789</catalogNumber><dunsNumber>463625602</dunsNumber><companyName>DIAGNOSTIC GRIFOLS SA</companyName><deviceCount>1</deviceCount><deviceDescription>WADiana Compact is a fully automated analyzer designed to automate in vitro immunohematological testing of human blood utilizing the DG Gel 8 cards technology. As a standalone or interfaced to the customer&apos;s Laboratory Information System (LIS), the WADiana Compact analyzer automates test processing functions and data management requirements using DG Gel 8 cards and digital image processing. </deviceDescription><DMExempt>false</DMExempt><premarketExempt>false</premarketExempt><deviceHCTP>false</deviceHCTP><deviceKit>false</deviceKit><deviceCombinationProduct>false</deviceCombinationProduct><singleUse>false</singleUse><lotBatch>false</lotBatch><serialNumber>true</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>(800)452-6877</phone><phoneExtension xsi:nil="true"/><email>service.americas@grifols.com</email></customerContact></contacts><gmdnTerms><gmdn><gmdnCode>56714</gmdnCode><gmdnPTName>Blood group/antibody screening analyser IVD</gmdnPTName><gmdnPTDefinition>An electrically-powered automated or semi-automated laboratory instrument intended to be used to perform pre-transfusion blood group testing, red cell antibody screening/identification and/or red cell phenotyping of clinical specimens or donor specimens in order to determine suitability for transfusion or transplantation. Testing may include ABO, Rhesus or other red cell blood group systems and may use microplate-based serological methods, cassettes or column agglutinating technology.</gmdnPTDefinition><implantable>false</implantable><gmdnCodeStatus>Active</gmdnCodeStatus></gmdn></gmdnTerms><productCodes><fdaProductCode><productCode>KSZ</productCode><productCodeName>System, Test, Automated Blood Grouping And Antibody</productCodeName></fdaProductCode></productCodes><deviceSizes/><environmentalConditions/><sterilization><deviceSterile>false</deviceSterile><sterilizationPriorToUse>false</sterilizationPriorToUse><methodTypes/></sterilization></device>