Nimbus

GUDID 10817170020007

Ambulatory infusion pump

INFUTRONIX LLC

Patient-controlled analgesia infusion pump

• Primary Device ID: 10817170020007
• NIH Device Record Key: 86196cae-3c1d-447a-8c75-70e4b429aa87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nimbus
• Version Model Number: Nimbus
• Company DUNS: 079821136
• Company Name: INFUTRONIX LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817170020000 [Primary]
GS1	10817170020007 [Package]; Contains: 00817170020000; Package: [24 Units]; In Commercial Distribution
GS1	20817170020004 [Package]; Contains: 00817170020000; Package: Inner pack [2 Units]; In Commercial Distribution
GS1	30817170020001 [Package]; Contains: 00817170020000; Package: Case [36 Units]; In Commercial Distribution

FDA Product Code

• MEA: Pump, Infusion, Pca

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [Nimbus]

• 00817170020154: This is a plastic box outside a drug bag less than or equal to 100ml.
• 10817170020106: Ambulaotry infusion pump
• 40817170020046: Administration set
• 40817170020039: Administration set
• 20817170020028: Administration Set
• 20817170020011: Administration set
• 10817170020007: Ambulatory infusion pump