{"publicDeviceRecordKey":"d39dfc65-a350-457c-884f-b7ae57ef6cdf","publicVersionStatus":"Update","deviceRecordStatus":"Published","publicVersionNumber":7,"publicVersionDate":"2026-05-21T00:00:00.000Z","devicePublishDate":"2017-06-12T00:00:00.000Z","deviceCommDistributionEndDate":"2025-09-03T00:00:00.000Z","deviceCommDistributionStatus":"Not in Commercial Distribution","identifiers":{"identifier":[{"deviceId":"50885403193543","deviceIdType":"Package","deviceIdIssuingAgency":"GS1","containsDINumber":"10885403193545","pkgQuantity":5,"pkgDiscontinueDate":"2025-09-03","pkgStatus":"Not in Commercial Distribution","pkgType":"Case"},{"deviceId":"10885403193545","deviceIdType":"Primary","deviceIdIssuingAgency":"GS1","containsDINumber":null,"pkgQuantity":null,"pkgDiscontinueDate":null,"pkgStatus":null,"pkgType":null}]},"brandName":"PleurX","versionModelNumber":"50-7290","catalogNumber":"50-7290","dunsNumber":"832696038","companyName":"CAREFUSION 2200, INC","deviceCount":1,"deviceDescription":"PleurX Procedure Pack","DMExempt":false,"premarketExempt":false,"deviceHCTP":false,"deviceKit":true,"deviceCombinationProduct":false,"singleUse":true,"lotBatch":true,"serialNumber":false,"manufacturingDate":false,"expirationDate":true,"donationIdNumber":false,"labeledContainsNRL":false,"labeledNoNRL":true,"MRISafetyStatus":"Labeling does not contain MRI Safety Information","rx":true,"otc":false,"contacts":{"customerContact":[{"phone":"+1(800)323-9088","phoneExtension":null,"email":"Customer_Support@BD.com"}]},"gmdnTerms":{"gmdn":[{"gmdnCode":"47797","gmdnPTName":"Pleural/peritoneal drainage catheterization kit, non-medicated","gmdnPTDefinition":"A collection of non-powered devices designed for catheterization of the pleural cavity and/or peritoneal cavity for drainage and/or aspiration of effusions (e.g., haemothorax, empyema, ascites), other fluids, and/or air; some types are additionally intended for infusion of fluids/materials into the pleural/peritoneal space. It includes a pleural catheter and/or a peritoneal catheter typically with catheter introduction devices (e.g., needles, scalpel, tunneller), non-dedicated catheterization support devices (e.g., dressings), drainage receptacle (e.g., collection bottle), and/or suction system regulator; it does not include any powered pumps or pharmaceuticals. This is a single-use device.","implantable":true,"gmdnCodeStatus":"Active"}]},"productCodes":{"fdaProductCode":[{"productCode":"DWM","productCodeName":"Apparatus, Suction, Patient Care"},{"productCode":"PNG","productCodeName":"Peritoneal, drainage catheter for refractory ascites, long-term indwelling"}]},"deviceSizes":{"deviceSize":[]},"environmentalConditions":{"storageHandling":[]},"sterilization":{"deviceSterile":true,"sterilizationPriorToUse":false,"methodTypes":{"sterilizationMethod":[]}},"xmlns":"http://www.fda.gov/cdrh/gudid","xsi":"http://www.w3.org/2001/XMLSchema-instance","anomaly":null,"premarketSubmissions":{"premarketSubmission":[]}}