Babi.Plus Babi-Plus nCPAP Nasal Prong Size 1

GUDID 44710810119710

GALEMED CORPORATION

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• Primary Device ID: 44710810119710
• NIH Device Record Key: 20b1f8ef-3244-4783-b087-6d30eb284f74
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Babi.Plus
• Version Model Number: B021
• Catalog Number: Babi-Plus nCPAP Nasal Prong Size 1
• Company DUNS: 656854379
• Company Name: GALEMED CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04710810119712 [Primary]
GS1	24710810119716 [Package]; Contains: 04710810119712; Package: box [20 Units]; Discontinued: 2015-12-31; Not in Commercial Distribution
GS1	44710810119710 [Package]; Contains: 24710810119716; Package: Carton [4 Units]; Discontinued: 2015-12-31; Not in Commercial Distribution

FDA Product Code

• CAT: Cannula, Nasal, Oxygen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-15

On-Brand Devices [Babi.Plus]

• 44710810093577: BC01-AU
• 44710810119741: B024
• 44710810119734: B023
• 44710810119727: B022
• 44710810119710: B021
• 44710810119703: B020
• 44710810100800: Distributed by Teleflex
• 44710810100794: Distributed by Teleflex
• 04710810093579: BC01-AU
• 44710810093560: BC23-AU
• 44710810117525: PA01
• 44710810093553: BC51-AU
• 04710810105265: BC01-AU