Pumpmatic

GUDID 00689519012058

205

Ashton Pumpmatic, Inc.

User-induced pipette

• Primary Device ID: 00689519012058
• NIH Device Record Key: efde44a0-b537-48f6-8798-1abcb2dcf7c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pumpmatic
• Version Model Number: 205
• Company DUNS: 007176126
• Company Name: Ashton Pumpmatic, Inc.
• Device Count: 25
• 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	00689519002059 [Primary]
GS1	00689519004053 [Primary]
GS1	00689519012058 [Unit of Use]

FDA Product Code

• GGY: PIPETTE, DILUTING

Sterilization

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

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