Amico Diagnostic Cuff

GUDID 00697077002633

Infant 2-Piece Cuff, 2 Tube LF, Orange, Infl Bulb x Screw Female

Amico Diagnostic Incorporated

Blood pressure cuff, reusable

• Primary Device ID: 00697077002633
• NIH Device Record Key: 9abd8592-84da-49ad-a79f-d593c481264a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amico Diagnostic Cuff
• Version Model Number: CR2-LF07O-2BVSM
• Company DUNS: 203163290
• Company Name: Amico Diagnostic Incorporated
• Device Count: 1
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com
• Phone: 1-877-462-6426
• Email: info@amico-accessories.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00697077002633 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K012444

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: 2025-03-06
• Device Publish Date: 2020-11-16

On-Brand Devices [Amico Diagnostic Cuff]

• 00697077002633: Infant 2-Piece Cuff, 2 Tube LF, Orange, Infl Bulb x Screw Female
• 00697077003074: Thigh 2-Piece Cuff, 2 Tubes LF, Brown, Infl Bulb x No Connector