Home GUDID 10886704028444 NA
Primary DI 10886704028444
Brand NA
Company Medos International Sàrl
Model 60-2918US
Catalog number 602918US
Device description Intraspinal Catheter Kit
Published 2014-09-20
Public version status Update
Distribution status Not in Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name LKK PUMP, INFUSION, IMPLANTED, PROGRAMMABLE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LKK Pump, Infusion, Implanted, Programmable Unknown 3
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10886704028444 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10886704028444 10886704028444
GMDN Terms# Term, Definition table Term Definition Spinal port/catheter A sterile implantable device intended to provide access to the subarachnoid (intrathecal) space of the spinal column for infusion (e.g., chemotherapeutic agents, pain relieving drugs) and/or drainage [e.g., cerebrospinal fluid (CSF)]. It consists of a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle, attached to a distal catheter which passes into the target site. It is made of metal [e.g., titanium (Ti)] and synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Temperature 15 Degrees Celsius 25 Degrees Celsius Handling Environment Temperature 59 Degrees Fahrenheit 77 Degrees Fahrenheit Special Storage Condition, Specify 0 0 Do not use if opened or damaged. Storage Environment Temperature 15 Degrees Celsius 25 Degrees Celsius Storage Environment Temperature 59 Degrees Fahrenheit 77 Degrees Fahrenheit
Regulatory Flags# DUNS number 482661753 Device count 1 Lot or batch true Expiration date on label true No natural rubber latex true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00199150021277 NA MEDTRONIC, INC. LKK 2026-05-02 00763000999414 SYNCHROMED™ III MEDTRONIC, INC. LKK 2026-01-15 00763000999421 SYNCHROMED™ III MEDTRONIC, INC. LKK 2026-01-15 00763000004101 NA MEDTRONIC, INC. LKK 2025-08-25 00763000574598 NA MEDTRONIC, INC. LKK 2025-02-10 00763000916633 NA MEDTRONIC, INC. LKK 2024-05-06 00763000916640 NA MEDTRONIC, INC. LKK 2024-05-06 00763000916657 Ascenda® MEDTRONIC, INC. LKK 2024-05-06 00763000916664 Ascenda® MEDTRONIC, INC. LKK 2024-05-03 00763000916671 Ascenda® MEDTRONIC, INC. LKK 2024-05-03 00763000825539 NA MEDTRONIC, INC. LKK 2024-03-30 00763000745073 NA MEDTRONIC, INC. LKK 2023-12-16 00763000597023 SYNCHROMED™ III MEDTRONIC, INC. LKK 2023-12-15 00763000597030 SYNCHROMED™ III MEDTRONIC, INC. LKK 2023-12-15 00763000825515 NA MEDTRONIC, INC. LKK 2023-12-09 00763000825522 NA MEDTRONIC, INC. LKK 2023-12-09 00763000852597 Ascenda® MEDTRONIC, INC. LKK 2023-12-09 00763000852603 Ascenda® MEDTRONIC, INC. LKK 2023-12-09 00763000852610 Ascenda® MEDTRONIC, INC. LKK 2023-12-09 00763000852627 Ascenda® MEDTRONIC, INC. LKK 2023-12-09 00763000852634 Ascenda® MEDTRONIC, INC. LKK 2023-12-09 00763000875725 NA MEDTRONIC, INC. LKK 2023-12-09 00763000875695 NA MEDTRONIC, INC. LKK 2023-11-16 00763000875701 NA MEDTRONIC, INC. LKK 2023-11-16 00763000875718 NA MEDTRONIC, INC. LKK 2023-11-16 00763000875862 N'VISION™ MEDTRONIC, INC. LKK 2023-11-16 00763000632786 NA MEDTRONIC, INC. LKK 2023-11-05 00763000632793 NA MEDTRONIC, INC. LKK 2023-11-05 00763000631482 NA MEDTRONIC, INC. LKK 2023-03-10 00763000301354 NA MEDTRONIC, INC. LKK 2022-10-09