PROCARE

GUDID 00840178700063

ProCare Emergency Code Response Cart

Touchpoint Medical, Inc.

Electromechanical device/system transport trolley

• Primary Device ID: 00840178700063
• NIH Device Record Key: 80f3b461-cb62-45e2-a964-ebeb4b7026f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROCARE
• Version Model Number: 120-002403-00
• Company DUNS: 080434935
• Company Name: Touchpoint Medical, Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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: false
• 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	00840178700063 [Primary]

FDA Product Code

• BZN: Cart, Emergency, Cardiopulmonary (Excluding Equipment)

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: 2024-04-09
• Device Publish Date: 2024-04-01

On-Brand Devices [PROCARE]

• 00840178700100: ProCare Intelligent Anesthesia Cart
• 00840178700094: ProCare Intelligent Procedure Cart
• 00840178700087: ProCare Anesthesia Cart
• 00840178700070: ProCare Pediatric Code Response Cart
• 00840178700063: ProCare Emergency Code Response Cart
• 00840178700056: ProCare General Procedure Cart, E-Lock
• 00840178700049: ProCare General Procedure Cart
• 00840178700032: ProCare Isolation Cart