E+R

GUDID B448FS1030

Firstar Healthcare Company Limited (Guangzhou)

Cardiopulmonary resuscitation mask, reusable

• Primary Device ID: B448FS1030
• NIH Device Record Key: 38890867-64a6-47d1-91f8-5f43a346f74a
• Commercial Distribution Discontinuation: 2023-08-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: E+R
• Version Model Number: FS-103
• Company DUNS: 529576331
• Company Name: Firstar Healthcare Company Limited (Guangzhou)
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B448FS1030 [Primary]

FDA Product Code

• CBP: Valve, Non-Rebreathing

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: 2023-09-08
• Device Publish Date: 2023-08-31

On-Brand Devices [E+R]

• 06942272610300: FS-103
• B448FS1030: FS-103