AngioJet® XMI® 105041

GUDID 08714729889151

Thrombectomy Set

BOSTON SCIENTIFIC CORPORATION

Thrombectomy suction catheter

• Primary Device ID: 08714729889151
• NIH Device Record Key: cbc10e1b-1fab-43b0-9bc5-ecfffc99af24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AngioJet® XMI®
• Version Model Number: 105041-001
• Catalog Number: 105041
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729889151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P980037

FDA Product Code

• MCX: CATHETER, CORONARY, ATHERECTOMY

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: 2022-08-05
• Device Publish Date: 2015-04-21

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 08714729037859 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729037873 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729037880 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729037927 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729037934 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729037996 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729038009 - Mardis Soft: 2025-05-19 Ureteral Stent Set
• 08714729038016 - Mardis Soft: 2025-05-19 Ureteral Stent Set