Sunmed Manifold and Stopcocks

GUDID 06947358551904

Sunny Medical Device (Shenzhen) Co., Ltd.

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• Primary Device ID: 06947358551904
• NIH Device Record Key: a02a2c80-8866-4f3a-aa55-e52cc3c0b25f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunmed Manifold and Stopcocks
• Version Model Number: 500psi, off hand
• Company DUNS: 529639795
• Company Name: Sunny Medical Device (Shenzhen) 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	06947358551904 [Primary]

FDA Product Code

• DTL: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

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: 2020-04-23
• Device Publish Date: 2020-04-15

Devices Manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.

• 06947358535539 - Sunmed™ guide wires: 2024-01-15
• 06947358563402 - Sunmed Inflation devices: 2023-10-03
• 06947358546719 - Sunmed Haemostatic Valves: 2023-07-14
• 06947358571698 - Sunmed disposable needles: 2023-07-14
• 06947358582618 - Sunmed disposable angio-closure pads: 2023-07-14
• 06947358544302 - Sunmed guidewire torque device: 2022-01-12
• 06947358566007 - Sunmed Inflation Device: 2022-01-12
• 06947358568001 - Sunmed Inflation Device: 2022-01-12