Guider Softip™ XF

GUDID 08714729283515

Guide Catheter

BOSTON SCIENTIFIC CORPORATION

Vascular guide-catheter, single-use

• Primary Device ID: 08714729283515
• NIH Device Record Key: 6d82e276-a55a-4e54-86bf-b03d99a3172b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guider Softip™ XF
• Version Model Number: M003100630
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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: true
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729283515 [Primary]

FDA Product Code

• DQY: CATHETER, PERCUTANEOUS

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: 2020-07-23
• Device Publish Date: 2016-09-24

On-Brand Devices [Guider Softip™ XF]

• 08714729283553: Guide Catheter
• 08714729283546: Guide Catheter
• 08714729283539: Guide Catheter
• 08714729283522: Guide Catheter
• 08714729283515: Guide Catheter
• 08714729283508: Guide Catheter
• 08714729244394: Guide Catheter
• 08714729244387: Guide Catheter
• 08714729244370: Guide Catheter
• 08714729244356: Guide Catheter
• 08714729244349: Guide Catheter
• 08714729244332: Guide Catheter
• 08714729244318: Guide Catheter
• 08714729244301: Guide Catheter
• 08714729244295: Guide Catheter
• 08714729202561: Guide Catheter
• 08714729202554: Guide Catheter
• 08714729202547: Guide Catheter
• 08714729202523: Guide Catheter
• 08714729202516: Guide Catheter
• 08714729202509: Guide Catheter
• 08714729202486: Guide Catheter
• 08714729202479: Guide Catheter
• 08714729202462: Guide Catheter