PICO™ 66022031

GUDID 05000223494391

PICO 7Y Single Use NPWT system

SMITH & NEPHEW MEDICAL LIMITED

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• Primary Device ID: 05000223494391
• NIH Device Record Key: f20e6e2f-f6e0-46e5-ab70-644f832fbf05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PICO™
• Version Model Number: 66022031
• Catalog Number: 66022031
• Company DUNS: 216344051
• Company Name: SMITH & NEPHEW MEDICAL LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05000223494391 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182323

FDA Product Code

• OMP: Negative Pressure Wound Therapy Powered Suction Pump

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: 2019-03-11
• Device Publish Date: 2019-02-26

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