bluejay

GUDID 06975185470051

Wenzhou Kangshun Medical Devices CO.,LTD

Aneroid manual sphygmomanometer

• Primary Device ID: 06975185470051
• NIH Device Record Key: 4b9eea96-880b-49a9-845c-3acee2b3f4c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: bluejay
• Version Model Number: BJ120200
• 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06975185470051 [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: 2024-06-17
• Device Publish Date: 2024-06-09

Devices Manufactured by Wenzhou Kangshun Medical Devices CO.,LTD

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