Pneupac

GUDID 10610586045479

ICU MEDICAL, INC.

Transport electric ventilator

• Primary Device ID: 10610586045479
• NIH Device Record Key: 289b2505-355b-4c73-9308-1de00f27ce84
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pneupac
• Version Model Number: 120002
• Company DUNS: 118380146
• Company Name: ICU MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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	10610586045479 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020899

FDA Product Code

• BTL: Ventilator, emergency, powered (resuscitator)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2025-04-16
• Device Publish Date: 2015-09-01

On-Brand Devices [Pneupac]

• 10610586045752: WW331002S
• 10610586045738: 520A1300US
• 10610586045721: 520A1299US
• 10610586045653: 150003V
• 10610586045622: 130002V
• 10610586045578: 150003
• 10610586045561: 130002
• 10610586045493: 122005
• 10610586045486: 120003
• 10610586045479: 120002
• 10610586038259: 130003