Sunmed disposable angio-closure pads

GUDID 06947358582618

Sunny Medical Device (Shenzhen) Co., Ltd.

Femoral artery compression bandage, single-use

• Primary Device ID: 06947358582618
• NIH Device Record Key: 30761c2e-a6bd-4150-b137-d40ce1fa8992
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunmed disposable angio-closure pads
• Version Model Number: Large Size
• Company DUNS: 529639795
• Company Name: Sunny Medical Device (Shenzhen) 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: 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	06947358582618 [Primary]

FDA Product Code

• DXC: Clamp, Vascular

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: 2023-07-14
• Device Publish Date: 2023-07-06

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
• 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