Home GUDID 00643169100824
SYNCHROMED ® II
Primary DI 00643169100824
Brand SYNCHROMED ® II
Company MEDTRONIC, INC.
Model 8637-40
Device description PUMP 8637-40 SYNCHMED II 40ML PF
Published 2016-04-27
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 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 00643169100824 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00643169100824 00643169100824 643169100824 0643169100824
GMDN Terms# Term, Definition table Term Definition Implantable intrathecal infusion pump, programmable A battery-powered programmable device designed to be implanted in a patient for the storing and subarachnoid (intrathecal) administration of narcotics/drugs (e.g., morphine sulfate, baclofen) to manage intractable pain and muscle spasms of malignant or non-malignant origin. This implantable infusion pump (IIP) delivers drug doses from its implanted refillable reservoir which is controlled by drug concentration and/or by radio-frequency (RF) signals from an external programming device. The drug reservoir, usually implanted under the skin of the lower abdomen, is typically connected to a catheter placed into the spinal fluid space.
Device Sizes# Type, Value, Unit table Type Value Unit Total Volume 0
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Temperature 0 0 Special Storage Condition, Specify 0 0 Keep away from Magnets
Regulatory Flags# DUNS number 006261481 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch false Serial number true Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false 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