RENASYS™ 66801271

GUDID 05000223497583

RENASYS TOUCH 800ml Canister without Solidifier case of 5

SMITH & NEPHEW MEDICAL LIMITED

Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister Negative-pressure wound therapy system canister

• Primary Device ID: 05000223497583
• NIH Device Record Key: 6cd38dfc-f5a1-4d85-a660-8314939d7fd3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENASYS™
• Version Model Number: 66801271
• Catalog Number: 66801271
• Company DUNS: 216344051
• Company Name: SMITH & NEPHEW MEDICAL LIMITED
• 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: false
• 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	05000223497576 [Primary]
GS1	05000223497583 [Package]; Contains: 05000223497576; Package: Case [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153209

FDA Product Code

• OMP: Negative Pressure Wound Therapy Powered Suction Pump

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: 2022-11-25
• Device Publish Date: 2022-11-17

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