W.A BAUM

GUDID 04560105682465

KENZMEDICO CO.,LTD.

Aneroid manual sphygmomanometer

• Primary Device ID: 04560105682465
• NIH Device Record Key: 6a83501c-f121-4cb5-8e90-213499c974fd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: W.A BAUM
• Version Model Number: No.500
• Company DUNS: 692910854
• Company Name: KENZMEDICO CO.,LTD.
• Device Count: 1
• 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: true
• 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	04560105682465 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K901506

FDA Product Code

• DXQ: Blood Pressure Cuff

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-20