T-SPeC 107

GUDID 08569950031073

Transurethral Suprapubic endo-Cystostomy

SWAN VALLEY MEDICAL, INCORPORATED

Suprapubic drainage catheter

• Primary Device ID: 08569950031073
• NIH Device Record Key: cdbb2f84-ab3a-4c3b-9bb8-8177d99b67b4
• Commercial Distribution Discontinuation: 2020-03-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: T-SPeC
• Version Model Number: T7
• Catalog Number: 107
• Company DUNS: 795608012
• Company Name: SWAN VALLEY MEDICAL, INCORPORATED
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 406-837-1500
• Email: cs@swanvalleymedical.com

Device Dimensions

• Catheter Gauge: 18 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	08569950031073 [Primary]

FDA Product Code

• FEX: Instrument, Catheter, Punch

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: 2020-04-01
• Device Publish Date: 2016-06-23

On-Brand Devices [T-SPeC]

• 00856995003010: Transurethral Suprapubic endo-Cystostomy
• 00856995003003: Transurethral Suprapubic endo-Cystostomy
• 08569950031141: Transurethral Suprapubic endo-Cystostomy
• 08569950031073: Transurethral Suprapubic endo-Cystostomy