DAYSPRING ARM GARMENT

GUDID 00850012532682

ARM GARMENT, DAYSPRING, MEDIUM

Koya Medical, Inc.

Wearable sequential venous compression system

• Primary Device ID: 00850012532682
• NIH Device Record Key: bffa115d-609d-4098-a3bf-5e0875dc6881
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DAYSPRING ARM GARMENT
• Version Model Number: F-0010-02
• Company DUNS: 100673310
• Company Name: Koya Medical, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012532682 [Primary]

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: 2023-09-28
• Device Publish Date: 2023-09-20

On-Brand Devices [DAYSPRING ARM GARMENT]

• 00850012532699: ARM GARMENT, DAYSPRING, LONG
• 00850012532682: ARM GARMENT, DAYSPRING, MEDIUM
• 00850012532675: ARM GARMENT, DAYSPRING, SHORT