WebModel Number LEAD1058-70B: Device Problem Adverse Event Without Identified Device or Use Problem (2993) Patient Problem Cerebrospinal Fluid Leakage (1772) Event Date 02/26/2024: Event Type Injury Manufacturer Narrative Web8 jun. 2024 · Brand Name: Nevro® Version or Model: LEAD1058-70B Commercial Distribution Status: In Commercial Distribution Catalog Number: LEAD1058-70B Company Name: NEVRO CORP. Primary DI Number: 00813426020046 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 1 Labeler D-U-N-S® Number*: …
University of New Mexico
WebModel Number LEAD1058-70B: Device Problem Detachment of Device or Device Component (2907) Patient Problem Device Embedded In Tissue or Plaque (3165) Event Date 09/30/2024: Event Type malfunction Manufacturer Narrative WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). form ac019
MAUDE Adverse Event Report: NEVRO CORP. SENZA NEVRO SENZA
WebHFX iQ is a smart pain management system that uses the largest clinical SCS dataset to recommend the starting program most likely to provide pain relief 1 and adjusts therapy based on each patient's responses to maintain optimized relief. 2 Learn more about HFX iQ Expanding Indications with HFX WebLEAD1058-70B: The version or model found on the device label or accompanying packaging used to identify a category or design of a device. The version or model identifies all devices that have specifications, performance, size, and composition within limits set by the labeler. Catalog Number: LEAD1058-70B WebLEAD1058-70B: Catalog Number: LEAD1058-70B: Company DUNS: 926599155: Company Name: NEVRO CORP. Device Count: 1: DM Exempt: false: Pre-market Exempt: false: MRI Safety Status: MR Conditional: Human Cell/Tissue Product: false: Device Kit: false: Device Combination Product: false: Single Use: true: Lot Batch: true: Serial … forma bwb mini bolo