Insufflator

GUDID 06971381251364

The insufflator is intended to form and maintain the pneumoperitoneum in laparoscopic surgery to provide visual field and operating space.

SCIVITA MEDICAL TECHNOLOGY CO., LTD.

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• Primary Device ID: 06971381251364
• NIH Device Record Key: 593a8620-3ddc-4f2e-945f-cb1c4115a3b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Insufflator
• Version Model Number: SL102
• Company DUNS: 544519831
• Company Name: SCIVITA MEDICAL TECHNOLOGY CO., LTD.
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	06971381251364 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222812

FDA Product Code

• HIF: Insufflator, Laparoscopic

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: 2024-03-07
• Device Publish Date: 2024-02-28

On-Brand Devices [Insufflator]

• 06971381251364: The insufflator is intended to form and maintain the pneumoperitoneum in laparoscopic surgery to
• 06971381251357: The insufflator is intended to form and maintain the pneumoperitoneum in laparoscopic surgery to