NBP Cuff XL, 38-50cm, Box10

GUDID 04048675042198

Drägerwerk AG & Co. KGaA

Blood pressure cuff, single-use

• Primary Device ID: 04048675042198
• NIH Device Record Key: e9a514f4-236f-4f02-bd83-a98f94152718
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NBP Cuff XL, 38-50cm, Box10
• Version Model Number: MP00934
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• Device Count: 10
• 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: false
• 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

Customer Support Contacts

• Phone: +494518820
• Email: info@draeger.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675042198 [Primary]
GS1	04048675428930 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092999

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: 2015-10-24

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