Millex-GP

GUDID 04054839076497

MERCK MILLIPORE LIMITED

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• Primary Device ID: 04054839076497
• NIH Device Record Key: 8b58b31c-b579-4e95-8a24-be08cd5940e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Millex-GP
• Version Model Number: SLGPM33RS
• Company DUNS: 896873994
• Company Name: MERCK MILLIPORE LIMITED
• Device Count: 50
• 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: true
• Expiration Date: true
• 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	04054839076497 [Primary]
GS1	04054839077982 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013988

FDA Product Code

• BSN: Filter, Conduction, Anesthetic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-22

Devices Manufactured by MERCK MILLIPORE LIMITED

• 04053252359194 - Multiscreen-HTS HV: 2023-10-23
• 04053252466274 - Multiscreen-HTS HV: 2023-10-23
• 04053252504501 - Multiscreen-HV: 2023-10-23
• 04053252505928 - Multiscreen-HV: 2023-10-23
• 04061839736382 - Amicon Ultra – 15: 2022-05-11
• 04061839736399 - Amicon Ultra – 4: 2022-05-11
• 04061839736405 - Amicon Ultra – 15: 2022-05-11
• 04061839736412 - Amicon Ultra – 4: 2022-05-11