MOCACARE

GUDID 00850842006292

MOCACARE CORP.

Public face mask, single-use

• Primary Device ID: 00850842006292
• NIH Device Record Key: 746831c9-5548-449d-ae40-22a7b4236279
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOCACARE
• Version Model Number: Procedure Mask
• Company DUNS: 079824513
• Company Name: MOCACARE CORP.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850842006292 [Primary]

FDA Product Code

• FXX: Mask, Surgical

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: 2023-05-08
• Device Publish Date: 2023-04-30

On-Brand Devices [MOCACARE]

• 00850842006308: Surgical Mask
• 00850842006292: Procedure Mask