PAEDIATRIC PLAIN INTERMITTENT CATHETER STRAIGHT TI

GUDID 05055788710608

FLEXICARE MEDICAL LIMITED

Urine-sampling urethral catheter

• Primary Device ID: 05055788710608
• NIH Device Record Key: 3f0beadb-32d0-412f-8b69-e211e384403d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PAEDIATRIC PLAIN INTERMITTENT CATHETER STRAIGHT TI
• Version Model Number: 03-50008U
• Company DUNS: 504406273
• Company Name: FLEXICARE 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: 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	05055788710608 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132619

FDA Product Code

• KOD: Catheter, Urological

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-10-04

On-Brand Devices [PAEDIATRIC PLAIN INTERMITTENT CATHETER STRAIGHT TI]

• 05055788710608: 03-50008U
• 05055788710592: 03-50010U