SHENGJIE

GUDID 06970614670347

Oxygen Tube

Weihai Shengjie Medical Technology Co., Ltd.

Oxygen administration tubing

• Primary Device ID: 06970614670347
• NIH Device Record Key: 8d8c7e84-3931-496a-9ad3-a16b1554a771
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SHENGJIE
• Version Model Number: M1
• Company DUNS: 530242002
• Company Name: Weihai Shengjie 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: 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	06970614670347 [Primary]

FDA Product Code

• BZB: Catheter, Nasal, Oxygen

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: 2026-03-10
• Device Publish Date: 2026-03-02

On-Brand Devices [SHENGJIE]

• 06970614670392: Oxygen Tube
• 06970614670385: Oxygen Tube
• 06970614670378: Oxygen Tube
• 06970614670361: Oxygen Tube
• 06970614670354: Oxygen Tube
• 06970614670347: Oxygen Tube
• 06970614670330: Oxygen Tube
• 06970614670323: Oxygen Tube
• 06970614670316: Oxygen Tube
• 06970614670309: Oxygen Tube