Air/Water Bottle Tubing

GUDID 06936534332260

Zhejiang Chuangxiang Medical Technology Co., LTD.

Endoscopic insufflation tubing set, single-use

• Primary Device ID: 06936534332260
• NIH Device Record Key: de4ae0ef-f329-47f6-8418-224ee336c8ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Air/Water Bottle Tubing
• Version Model Number: MD-B-SE-70212
• Company DUNS: 544434963
• Company Name: Zhejiang Chuangxiang 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06936534332260 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231471

FDA Product Code

• OCX: Endoscopic Irrigation/Suction System

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: 2023-12-26
• Device Publish Date: 2023-12-18

On-Brand Devices [Air/Water Bottle Tubing]

• 06936534332253: MD-A-SE-70012
• 06936534332260: MD-B-SE-70212