Closed Suction System for Adult

GUDID 06959180703727

VR Medical Technology Co., Ltd.

Tracheostomy tube cuff

• Primary Device ID: 06959180703727
• NIH Device Record Key: aa01166f-c085-4f40-88f9-cb8dc22baca1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Closed Suction System for Adult
• Version Model Number: VR04214US
• Company DUNS: 420798349
• Company Name: VR Medical Technology Co., Ltd.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• 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
GS1	06959180703727 [Primary]

FDA Product Code

• BSY: Catheters, Suction, Tracheobronchial

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-04-09
• Device Publish Date: 2018-03-08

Devices Manufactured by VR Medical Technology Co., Ltd.

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• 16959180731987 - VR Medical Technology Co., Ltd.: 2024-08-27 Closed suction System ,VR041606
• 16959180753194 - VR Medical Technology Co., Ltd.: 2024-08-27 Closed suction System ,VR041607
• 16959180703731 - Closed Suction System: 2020-05-14
• 16959180704219 - Closed Suction System: 2020-05-14
• 16959180704318 - Closed Suction System: 2020-05-14
• 16959180704332 - Closed Suction System: 2020-05-14