konsunmed

GUDID 06975185470068

Wenzhou Kangshun Medical Devices CO.,LTD

Aneroid manual sphygmomanometer

• Primary Device ID: 06975185470068
• NIH Device Record Key: eced0a44-bae4-412f-a8f1-72a1903fcbb8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: konsunmed
• Version Model Number: 01
• Company DUNS: 544394159
• Company Name: Wenzhou Kangshun Medical Devices CO.,LTD
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975185470068 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230859

FDA Product Code

• DXQ: Blood Pressure Cuff

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: 2024-07-11
• Device Publish Date: 2024-07-03

Devices Manufactured by Wenzhou Kangshun Medical Devices CO.,LTD

• 06975185470068 - konsunmed: 2024-07-11
• 06975185470068 - konsunmed: 2024-07-11
• 06975185470051 - bluejay: 2024-06-17