Home GUDID 78888893011102 Biosensors Central Venous Catheter Kit
Primary DI 78888893011102
Brand Biosensors Central Venous Catheter Kit
Company BIOPTIMAL INTERNATIONAL PTE. LTD.
Model CVR-501-16
Catalog number 25-000009-49
Published 2016-09-01
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name FOZ Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 28888893011107 Package GS1 10 In Commercial Distribution 78888893011102 Package GS1 8 In Commercial Distribution 08888893011103 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 28888893011107 28888893011107 78888893011102 78888893011102 08888893011103 08888893011103 8888893011103
GMDN Terms# Term, Definition table Term Definition Central venous catheterization kit, short-term A collection of sterile devices and materials intended for the short-term (<= 30 days) introduction of a central venous catheter (CVC) for various infusion/aspiration procedures (i.e., non-dedicated). Often referred to as tray, it includes a nonimplantable central venous catheter with devices dedicated to catheter introduction/function (e.g., introducer, guidewire), and non-dedicated supportive devices (e.g., drape, dressings, scalpel). This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store in dark cool dry places
Regulatory Flags# DUNS number 595182247 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 08886483551640 Thermodilution Catheter and Accessories TD1755HD 21-000153-50 2026-05-20 08886483551657 Thermodilution Catheter and Accessories TD2755NDF 21-000202-45 2026-05-20 08886483551664 Safewedge(TM) Relief Valve Device Safetywedge 21-000212-01 2026-05-20 08886483500174 Thermodilution Catheter and Accessories TD2604NXF 21-000009-58 2026-05-04 08886483500181 Thermodilution Catheter and Accessories TD2604NDXF 21-000009-59 2026-05-04 08886483500372 Thermodilution Catheter and Accessories TD2504NXF 21-000046-43 2026-05-04 08886483500389 Thermodilution Catheter and Accessories TD2504NDXF 21-000046-44 2026-05-04 08886483501508 Thermodilution Catheter and Accessories TD2704NDF 21-000201-16 2026-05-04 08886483501515 Thermodilution Catheter and Accessories TD2704NCXF 21-000201-17 2026-05-04 08886483501546 Thermodilution Catheter and Accessories TD2755NX 21-000202-00 2026-05-04 08886483501553 Thermodilution Catheter and Accessories TD2755NDF 21-000202-01 2026-05-04 08886483501577 Thermodilution Catheter and Accessories TD2755NDX 21-000202-03 2026-05-04 08886483501584 Thermodilution Catheter and Accessories TD2755NDPXF 21-000202-04 2026-05-04 08886483502390 BIOTRANS™ Pressure Monitoring Kits BTR4812-3 22-000813-23 2026-05-04 08886483503151 BIOTRANS™ Pressure Monitoring Kits EXTENSION TUBING SET 22-000895-96 2026-05-04 08886483503748 ACCUTRANS Disposable Pressure Monitoring Kit AT W/O IFU(BNS) 22-000940-02 2026-05-04 08886483504455 Embolectomy Catheter EL1440 23-000006-15 2026-05-04 08886483504486 Embolectomy Catheter EL1580 23-000006-18 2026-05-04 08886483504516 Embolectomy Catheter EL1540 23-000006-21 2026-05-04 08886483507005 BIOTRANS™ Reusable Sensor Base and Monitor Adapter Cables BT-201 BL-0003-018 2026-05-04
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