Amplatz Super Stiff

GUDID 08714729191193

Guidewire

BOSTON SCIENTIFIC CORPORATION

Gastro-urological guidewire, single-use

• Primary Device ID: 08714729191193
• NIH Device Record Key: f1e52170-9bd5-4e38-9653-c6a6eab07e00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Amplatz Super Stiff
• Version Model Number: M0066401090
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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: 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729191193 [Package]; Contains: 08714729752714; Package: [5 Units]; In Commercial Distribution
GS1	08714729752714 [Primary]

FDA Product Code

• EZB: STYLET FOR CATHETER, GASTRO-UROLOGY

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-12-23
• Device Publish Date: 2016-09-24

On-Brand Devices [Amplatz Super Stiff]

• 08714729301929: Guidewire
• 08714729191193: Guidewire
• 08714729191186: Guidewire
• 08714729191179: Guidewire
• 08714729191162: Guidewire
• 08714729191155: Guidewire
• 08714729191148: Guidewire