SINGLE USE INFANT 280ML RESUSCITATOR W/ POP-OFF 4

GUDID 04716770256207

BESMED HEALTH BUSINESS CORP.

Pulmonary resuscitator, manual, single-use

• Primary Device ID: 04716770256207
• NIH Device Record Key: 918ea988-614c-4b16-b8f0-7b3e313ed7f6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SINGLE USE INFANT 280ML RESUSCITATOR W/ POP-OFF 4
• Version Model Number: RE-25620
• Company DUNS: 658023775
• Company Name: BESMED HEALTH BUSINESS 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04716770256207 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021442

FDA Product Code

• BTM: Ventilator, Emergency, Manual (Resuscitator)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-05-23

On-Brand Devices [ SINGLE USE INFANT 280ML RESUSCITATOR W/ POP-OFF 4]

• 04716770256207: RE-25620
• 04716770236100: RE-23610
• 04716770226255: RE-22625