SecurAcath 400110

GUDID 10865382000225

INTERRAD MEDICAL, INC

Wearable percutaneous catheter/tube holder

• Primary Device ID: 10865382000225
• NIH Device Record Key: 8aecbda2-b4b4-4258-a1f0-23bd4d14d889
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SecurAcath
• Version Model Number: 5F
• Catalog Number: 400110
• Company DUNS: 555472310
• Company Name: INTERRAD MEDICAL, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Catheter Gauge: 5 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00865382000228 [Primary]
GS1	10865382000225 [Package]; Contains: 00865382000228; Package: Shelf Box [10 Units]; In Commercial Distribution

FDA Product Code

• LJS: Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-07-22
• Device Publish Date: 2016-09-15

On-Brand Devices [SecurAcath]

• 10865382000256: 8F
• 10865382000249: 7F
• 10865382000232: 6F
• 10865382000225: 5F
• 10865382000218: 4F
• 10865382000201: 3F
• 00865382000297: 10F
• 00865382000280: 12F