BluFlex

GUDID 64719873230008

Intermittent venous compression system (Pump)

PEGASUS MEDICAL SUPPLY, INC.

Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system

• Primary Device ID: 64719873230008
• NIH Device Record Key: dcf15730-aefb-4d98-8762-b8252839c630
• Commercial Distribution Discontinuation: 2021-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BluFlex
• Version Model Number: M6
• Company DUNS: 656766271
• Company Name: PEGASUS MEDICAL SUPPLY, 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719873230006 [Primary]
GS1	64719873230008 [Package]; Contains: 04719873230006; Package: BOX [6 Units]; Discontinued: 2021-12-31; In Commercial Distribution

FDA Product Code

• JOW: Sleeve, Limb, Compressible

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: 2017-07-19

On-Brand Devices [BluFlex]

• 14719873230133: Intermittent venous compression system (Tubing)
• 14719873230126: Intermittent venous compression system (Tubing)
• 04719873230112: Intermittent venous compression system (Tubing)
• 14719873230102: Intermittent venous compression system (Tubing)
• 64719873230091: Intermittent venous compression system (Sleeves)
• 64719873230084: Intermittent venous compression system (Sleeves)
• 24719873230079: Intermittent venous compression system (Sleeves)
• 24719873230062: Intermittent venous compression system (Sleeves)
• 24719873230055: Intermittent venous compression system (Sleeves)
• 24719873230048: Intermittent venous compression system (Sleeves)
• 44719873230035: Intermittent venous compression system (Sleeves)
• 44719873230028: Intermittent venous compression system (Sleeves)
• 44719873230011: Intermittent venous compression system (Sleeves)
• 64719873230008: Intermittent venous compression system (Pump)