NBP Cuff L+, 31-40/55cm, Box10

GUDID 04048675428947

Drägerwerk AG & Co. KGaA

Blood pressure cuff, single-use

• Primary Device ID: 04048675428947
• NIH Device Record Key: b67129d8-46e8-44a3-9480-6a8ad5a79fe1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NBP Cuff L+, 31-40/55cm, Box10
• Version Model Number: MP00932
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675042174 [Primary]
GS1	04048675428947 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-06-30
• Device Publish Date: 2022-06-22

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