Graseby

GUDID 30610586021712

ICU MEDICAL, INC.

Mechanical pipette

• Primary Device ID: 30610586021712
• NIH Device Record Key: a075f507-ca21-433c-8700-e9476375a8cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Graseby
• Version Model Number: 21-0402-25
• Company DUNS: 118380146
• Company Name: ICU MEDICAL, INC.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10610586021718 [Primary]
GS1	30610586021712 [Package]; Contains: 10610586021718; Package: BOX [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K894360

FDA Product Code

• FRN: Pump, infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2025-04-16
• Device Publish Date: 2016-10-13

On-Brand Devices [Graseby]

• 30610586022672: 21-0440-25
• 30610586022658: 21-0442-25
• 30610586022634: 21-0440-25
• 30610586022375: 21-0425-01
• 30610586021712: 21-0402-25