Graseby

GUDID 30610586100172

SMITHS MEDICAL MD, INC.

Mechanical pipette

• Primary Device ID: 30610586100172
• NIH Device Record Key: 08736347-a0e4-48e2-b202-3b6400667eb7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Graseby
• Version Model Number: 21-0316-25
• Company DUNS: 106712748
• Company Name: SMITHS MEDICAL MD, 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	00610586100171 [Primary]
GS1	30610586100172 [Package]; Contains: 00610586100171; Package: BOX [30 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: 4
• Public Version Date: 2018-08-17
• Device Publish Date: 2016-10-13

On-Brand Devices [Graseby]

• 30610586100509: 21-0349-25
• 30610586100486: 21-0347-25
• 30610586100479: 21-0346-25
• 30610586100462: 21-0345-25
• 30610586100196: 21-0318-25
• 30610586100189: 21-0317-25
• 30610586100172: 21-0316-25