Centriprep-30K

GUDID 04054839076237

MERCK MILLIPORE LIMITED

Laboratory dialyser

• Primary Device ID: 04054839076237
• NIH Device Record Key: c1b6ad4b-9efd-4c46-8a2b-0136ba0a2ada
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centriprep-30K
• Version Model Number: 4307
• Company DUNS: 896873994
• Company Name: MERCK MILLIPORE LIMITED
• Device Count: 96
• 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	04054839076237 [Primary]
GS1	04054839077050 [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-30K]

• 04054839076237: 4307
• 04054839076183: 4306