CPR Bag

GUDID 30641043542204

MERCURY ENTERPRISES, INC.

Pulmonary resuscitator, manual, single-use

• Primary Device ID: 30641043542204
• NIH Device Record Key: dfffdee5-63e2-43e0-9160-b47bf46e39f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CPR Bag
• Version Model Number: 10-54220
• Company DUNS: 032705659
• Company Name: MERCURY ENTERPRISES, INC.
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (727) 573-0088
• Email: hospitalcustomerservice@mercurymed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10641043542200 [Primary]
GS1	30641043542204 [Package]; Contains: 10641043542200; Package: [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K911622

FDA Product Code

• BTM: Ventilator, Emergency, Manual (Resuscitator)

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: 2019-11-25
• Device Publish Date: 2019-11-15

On-Brand Devices [CPR Bag]

• 30641043587007: 10-58700
• 10641043557181: 10-55718
• 30641043559301: 10-55930
• 30641043542204: 10-54220
• 30641043559318: 10-55931
• 30641043557192: 10-55719
• 30641043542211: 10-54221
• 30641043541122: 10-54112
• 30641043541115: 10-54111
• 30641043552005: 10-55200