CLR Medical S012-01-200

GUDID 00860003054949

CLR Medical

Closed-wound drain connector

• Primary Device ID: 00860003054949
• NIH Device Record Key: ef1f899d-4d4f-412d-95fd-6c9ceb6ba89f
• Commercial Distribution Discontinuation: 2024-09-22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLR Medical
• Version Model Number: CLR Irrigation & Drainage Kit
• Catalog Number: S012-01-200
• Company DUNS: 080279373
• Company Name: CLR Medical
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860003054949 [Primary]
GS1	00860003054970 [Package]; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• PXU: Fluid Drainage Tray

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: 2021-11-15
• Device Publish Date: 2021-11-05

Devices Manufactured by CLR Medical

• 00850052377021 - CLR Port Injector: 2024-06-06
• 00860003054901 - CLR Irrigator: 2024-06-06
• 00860003054956 - CLR Port: 2024-06-06
• 00850052377014 - CLR Port Cap: 2024-06-06
• 00860003054949 - CLR Medical: 2021-11-15
• 00860003054949 - CLR Medical: 2021-11-15