Centrifree

GUDID 04054839076046

MERCK MILLIPORE LIMITED

Laboratory dialyser

• Primary Device ID: 04054839076046
• NIH Device Record Key: c5e9a31c-0fd4-4b8a-8b3c-0a32050aead7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centrifree
• Version Model Number: 4104
• Company DUNS: 896873994
• Company Name: MERCK MILLIPORE LIMITED
• Device Count: 50
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04054839076046 [Primary]
GS1	04054839077890 [Unit of Use]

FDA Product Code

• JJH: Clinical Sample Concentrator

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

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