Sequential Circulator

GUDID 00812311021373

Bio Compression Systems, Inc

Sequential venous compression system pump

• Primary Device ID: 00812311021373
• NIH Device Record Key: f692e3f2-b282-4911-90e6-a496ce14aa6c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sequential Circulator
• Version Model Number: SC-3008-T-230
• Company DUNS: 101393924
• Company Name: Bio Compression Systems, 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	00812311021373 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K043423

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: 2019-02-18
• Device Publish Date: 2019-01-17

On-Brand Devices [Sequential Circulator]

• 00812311021373: SC-3008-T-230
• 00812311026484: SC-4008-DL
• 00812311026446: SC-4004-DL
• 00812311026286: SC-2008-DL
• 00812311026248: SC-2004-DL
• 00812311026187: SC-1008-DL
• 00812311026149: SC-1004-DL