Adapter , Box10

GUDID 04048675267706

Drägerwerk AG & Co. KGaA

Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable Non-ISO80369-standardized small-bore linear connector, reusable

• Primary Device ID: 04048675267706
• NIH Device Record Key: ebe1e73f-6916-474a-bf0c-5b5bb805a579
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Adapter , Box10
• Version Model Number: MP00945
• 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: false
• Lot Batch: true
• Serial Number: false
• 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	04048675267706 [Primary]
GS1	04048675448419 [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: 2
• Public Version Date: 2023-03-23
• Device Publish Date: 2022-06-17

On-Brand Devices [Adapter , Box10]

• 04048675448419: MP00945
• 04048675267706: MP00945