Sil.Plus pedi-Circuit w/water trap

GUDID 44710810119192

GALEMED CORPORATION

Anaesthesia breathing circuit, reusable

• Primary Device ID: 44710810119192
• NIH Device Record Key: 042a3db0-7679-4db9-b41a-521710b14b98
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sil.Plus
• Version Model Number: B111
• Catalog Number: pedi-Circuit w/water trap
• 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	24710810119198 [Primary]
GS1	44710810119192 [Package]; Contains: 24710810119198; Package: Carton [6 Units]; In Commercial Distribution

FDA Product Code

• CAI: Circuit, Breathing (W Connector, Adaptor, Y Piece)

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 [Sil.Plus]

• 44710810119192: B111
• 44710810117105: B121