Centriprep-10K

GUDID 04054839076169

MERCK MILLIPORE LIMITED

Laboratory dialyser

• Primary Device ID: 04054839076169
• NIH Device Record Key: b2d33c0d-f1a3-4d4a-b043-5585027e1975
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centriprep-10K
• Version Model Number: 4304
• 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	04054839076169 [Primary]
GS1	04054839077791 [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

On-Brand Devices [Centriprep-10K]

• 04054839076220: 4305
• 04054839076169: 4304