HME-Booster T-piece WFL + Hygrovent S HMEF

GUDID 05055788790259

FLEXICARE MEDICAL LIMITED

Heat/moisture exchanger/microbial filter, non-sterile

• Primary Device ID: 05055788790259
• NIH Device Record Key: f8cbb9f2-3f36-4fbc-85ec-ccc4c66e490f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HME-Booster T-piece WFL + Hygrovent S HMEF
• Version Model Number: 362-200-000
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055788790259 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122885

FDA Product Code

• BTT: Humidifier, Respiratory Gas, (Direct Patient Interface)

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: 2020-04-06
• Device Publish Date: 2020-03-27

On-Brand Devices [HME-Booster T-piece WFL + Hygrovent S HMEF]

• 05055788792345: 362-200-000U
• 05055788790259: 362-200-000