SecurAcath 400130

GUDID 10865382000201

INTERRAD MEDICAL, INC

Wearable percutaneous catheter/tube holder

• Primary Device ID: 10865382000201
• NIH Device Record Key: 6f7a6b3b-7a9b-4383-adb8-7f0db5fc39cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SecurAcath
• Version Model Number: 3F
• Catalog Number: 400130
• 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: 3 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00865382000204 [Primary]
GS1	10865382000201 [Package]; Contains: 00865382000204; Package: Shelf Box [10 Units]; In Commercial Distribution

FDA Product Code

• OKC: Implanted Subcutaneous Securement Catheter

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