NuStat Trauma Pad

GUDID 00850392006551

BEEKEN BIOMEDICAL LLC

Wound dressing kit, non-medicated, sterile

• Primary Device ID: 00850392006551
• NIH Device Record Key: 1774d096-142f-4b08-b8a0-2ba04abf3e91
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuStat Trauma Pad
• Version Model Number: N-0236
• Company DUNS: 028807882
• Company Name: BEEKEN BIOMEDICAL LLC
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850392006551 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160578

FDA Product Code

• FRO: Dressing, Wound, Drug

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: 2021-01-18
• Device Publish Date: 2021-01-08

Devices Manufactured by BEEKEN BIOMEDICAL LLC

• 10850392006169 - NuStat XR: 2024-02-28
• 00850392006100 - NuStat Flex: 2023-05-12 NuStat Flex hemostatic wound dressing
• 00850392006155 - NuStat: 2023-03-09 NuStat 4x4
• 00850392006018 - NuStat: 2022-11-28
• 00850392006179 - NuStat Trauma Pad XR: 2021-01-18
• 00850392006223 - NuStat Flex XR: 2021-01-18
• 00850392006230 - NuStat Flex XR: 2021-01-18
• 00850392006247 - NuStat Flex XR: 2021-01-18