{"publicDeviceRecordKey":"0eddab9f-156e-4dd7-be1b-15bd4e4fdb3e","publicVersionStatus":"Update","deviceRecordStatus":"Published","publicVersionNumber":2,"publicVersionDate":"2026-02-09T00:00:00.000Z","devicePublishDate":"2023-07-18T00:00:00.000Z","deviceCommDistributionEndDate":null,"deviceCommDistributionStatus":"In Commercial Distribution","identifiers":{"identifier":[{"deviceId":"00850291007369","deviceIdType":"Primary","deviceIdIssuingAgency":"GS1","containsDINumber":null,"pkgQuantity":null,"pkgDiscontinueDate":null,"pkgStatus":null,"pkgType":null}]},"brandName":"InThrill Sheath","versionModelNumber":"53-101","catalogNumber":"53-101","dunsNumber":"076827459","companyName":"Inari Medical, Inc.","deviceCount":1,"deviceDescription":"InThrill Sheath (InThrill Thrombectomy System)","DMExempt":false,"premarketExempt":false,"deviceHCTP":false,"deviceKit":false,"deviceCombinationProduct":false,"singleUse":true,"lotBatch":true,"serialNumber":false,"manufacturingDate":false,"expirationDate":true,"donationIdNumber":false,"labeledContainsNRL":false,"labeledNoNRL":false,"MRISafetyStatus":"Labeling does not contain MRI Safety Information","rx":true,"otc":false,"contacts":{"customerContact":[{"phone":"877-923-4747","phoneExtension":null,"email":"info@inarimedical.com"}]},"premarketSubmissions":{"premarketSubmission":[{"submissionNumber":"K220887","supplementNumber":"000"},{"submissionNumber":"K223613","supplementNumber":"000"}]},"gmdnTerms":{"gmdn":[{"gmdnCode":"66423","gmdnPTName":"Thrombectomy wire-net introduction set","gmdnPTDefinition":"A dedicated collection of manual invasive devices intended to provide percutaneous vascular access to enable the introduction, and safe retrieval, of a thrombectomy wire-net (not included) during a thrombectomy procedure. It includes a non-steerable sheath typically with an expanding distal funnel to facilitate wire-net retrieval, an obturator/dilator, a haemostatic valve to control blood loss, and a side port. It is typically also designed to allow removal of residual clotted blood, trapped in the sheath funnel upon retrieval, through manual suction (aspiration). This is a single-use device.","implantable":false,"gmdnCodeStatus":"Active"}]},"productCodes":{"fdaProductCode":[{"productCode":"KRA","productCodeName":"Catheter, Continuous Flush"},{"productCode":"QEW","productCodeName":"Peripheral Mechanical Thrombectomy With Aspiration"}]},"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}