Amicon Ultra – 15

GUDID 04061839736429

MERCK MILLIPORE LIMITED

Laboratory dialyser

• Primary Device ID: 04061839736429
• NIH Device Record Key: 19879127-9b33-48fd-bfc1-063d084d6a1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amicon Ultra – 15
• Version Model Number: UFC901024D
• Company DUNS: 896873994
• Company Name: MERCK MILLIPORE LIMITED
• Device Count: 24
• 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	04061839736429 [Primary]
GS1	04061841163169 [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: 2022-05-11
• Device Publish Date: 2019-10-08

On-Brand Devices [Amicon Ultra – 15]

• 04054839076800: UFC901008
• 04054839076640: UFC901096
• 04054839076633: UFC901024
• 04061839736429: UFC901024D
• 04061839736405: UFC901096D
• 04061839736382: UFC901008D