Compressible Limb Therapy System(MK300L)

GUDID 28809315679118

6 chamber ARM EXTENSION ZIPPER (One size)

DAESUNG MAREF CO.,LTD.

Pneumatic massager

• Primary Device ID: 28809315679118
• NIH Device Record Key: 47dce79f-751e-47d8-8298-b92d7b34f466
• Commercial Distribution Discontinuation: 2023-03-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Compressible Limb Therapy System(MK300L)
• Version Model Number: ACg0631
• Company DUNS: 688817949
• Company Name: DAESUNG MAREF CO.,LTD.
• Device Count: 2
• 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: 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	08809315679107 [Unit of Use]
GS1	08809315679114 [Primary]
GS1	18809315679111 [Package]; Contains: 08809315679114; Package: BOX [20 Units]; Discontinued: 2023-03-21; Not in Commercial Distribution
GS1	28809315679118 [Package]; Contains: 08809315679114; Package: BOX [40 Units]; Discontinued: 2023-03-21; Not in Commercial Distribution

FDA Product Code

• IRP: Massager, Powered Inflatable Tube

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2023-03-22
• Device Publish Date: 2016-10-24

On-Brand Devices [Compressible Limb Therapy System(MK300L)]

• 28809315679132: 6 chamber FULL BODY EXTENSION ZIPPER (One size)
• 28809315679118: 6 chamber ARM EXTENSION ZIPPER (One size)
• 28809315679095: 6 chamber LEG EXTENSION ZIPPER (Extra large)
• 28809315679071: 6 chamber LEG EXTENSION ZIPPER (Large)