ActiveCare® DVT A502B000105

GUDID 00889024504622

ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.

Sequential venous compression system pump

• Primary Device ID: 00889024504622
• NIH Device Record Key: 63fea41c-da82-48ef-9bbb-5dfe7a510e43
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ActiveCare® DVT
• Version Model Number: A502B000105
• Catalog Number: A502B000105
• Company DUNS: 137354267
• Company Name: ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024504622 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140755

FDA Product Code

• JOW: SLEEVE, LIMB, COMPRESSIBLE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-04
• Device Publish Date: 2019-02-01

On-Brand Devices [ActiveCare® DVT]

• 00889024504653: A502B000111
• 00889024504646: A502B000109
• 00889024504622: A502B000105
• 00889024504615: A502B000103
• 00889024504530: A502B000102