FMS2000 ACCESSORY

GUDID 20896128002033

FMS2000 ACCESSORY, IV Pole

BELMONT INSTRUMENT CORPORATION

Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump Warming/high-flow infusion pump

• Primary Device ID: 20896128002033
• NIH Device Record Key: 3b0d13c3-c5c9-41ad-9b20-e9e23557e14b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FMS2000 ACCESSORY
• Version Model Number: 903-00013
• Company DUNS: 078330362
• Company Name: BELMONT INSTRUMENT CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	20896128002033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091855

FDA Product Code

• FRN: Pump, Infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

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