AccessGUDID - DEVICE: SYNCHROMED ® II (00613994779229)

GUDID

Device Identifier (DI) Information

Brand Name: SYNCHROMED ® II
Version or Model: 8637-20
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: MEDTRONIC, INC.

Primary DI Number: 00613994779229
Issuing Agency: GS1
Commercial Distribution End Date: October 25, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 796986144 *Terms of Use

Device Description: PUMP 8637-20 SM2 20ML EMAN US JUN BATRY

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Implantable intrathecal infusion pump, programmable	A battery-powered, programmable, sterile 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 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.

GMDN Preferred Term Name

GMDN Definition

Implantable intrathecal infusion pump, programmable

A battery-powered, programmable, sterile 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 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.

FDA Product Code

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Product Code	Product Code Name
LKK	PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P860004	130

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

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Storage and Handling
Special Storage Condition, Specify: Keep away from Magnets
Handling Environment Temperature: between 41 and 110 Degrees Fahrenheit
Handling Environment Temperature: between 5 and 43 Degrees Celsius

Clinically Relevant Size

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Size Type Text
Total Volume: 20.0 Milliliter

Device Record Status

Public Device Record Key: 9698bdb3-661b-4900-919f-2d130abf8d75
Public Version Date: December 23, 2022
Public Version Number: 4
DI Record Publish Date: April 27, 2016