SINGLE USE ADULT 1000ML RESUSCITATOR W/O POP-OFF ,

GUDID 04716770234335

BESMED HEALTH BUSINESS CORP.

Pulmonary resuscitator, manual, single-use

• Primary Device ID: 04716770234335
• NIH Device Record Key: 8da65a4e-731d-474b-baa9-fd9843cd56f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SINGLE USE ADULT 1000ML RESUSCITATOR W/O POP-OFF ,
• Version Model Number: RE-23433
• 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	04716770234335 [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: 2016-06-03

On-Brand Devices [SINGLE USE ADULT 1000ML RESUSCITATOR W/O POP-OFF ,]

• 04716770234335: RE-23433
• 04716770234328: RE-23432