Pumpmatic

GUDID 00689519017015

701

Ashton Pumpmatic, Inc.

User-induced pipette

• Primary Device ID: 00689519017015
• NIH Device Record Key: 79b74abe-7705-40dd-980e-ee0b0413671d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pumpmatic
• Version Model Number: 701
• Company DUNS: 007176126
• Company Name: Ashton Pumpmatic, Inc.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00689519007016 [Primary]
GS1	00689519017015 [Unit of Use]

FDA Product Code

• GGY: PIPETTE, DILUTING

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-22
• Device Publish Date: 2023-12-14

On-Brand Devices [Pumpmatic]

• 00689519017015: 701
• 00689519012102: 210
• 00689519012058: 205
• 00689519012010: 201
• 00689519011105: 110
• 00689519011051: 105
• 00689519011013: 101
• 00689519031103: 1-110
• 00689519031059: 1-105
• 00689519031011: 1-101