Welby

GUDID 10697038425621

HONSUN (NANTONG) CO.,LTD

Automatic-inflation electronic sphygmomanometer, portable, finger

• Primary Device ID: 10697038425621
• NIH Device Record Key: b848cf5d-3297-4afc-96aa-20bf98b87aec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Welby
• Version Model Number: LD-753
• Company DUNS: 543364560
• Company Name: HONSUN (NANTONG) CO.,LTD
• Device Count: 5
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00697038425624 [Unit of Use]
GS1	10697038425621 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131463

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-08
• Device Publish Date: 2018-02-03

On-Brand Devices [Welby]

• 00697038425624: LD-753
• 10697038425621: LD-753