Millex-HA

GUDID 04054839076596

MERCK MILLIPORE LIMITED

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• Primary Device ID: 04054839076596
• NIH Device Record Key: 0bddfd39-8a68-472d-a9a8-891917d8e1cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Millex-HA
• Version Model Number: SLHAM33SS
• 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	04054839076596 [Primary]
GS1	04054839078248 [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

On-Brand Devices [Millex-HA]

• 04054839076626: SLHA02510
• 04054839076596: SLHAM33SS