GUDID 08714729005278

Malecot Nephrostomy Catheter Set

BOSTON SCIENTIFIC CORPORATION

Nephrostomy catheter

• Primary Device ID: 08714729005278
• NIH Device Record Key: c3077d33-df39-4963-9e1f-000bf74f3e1f
• Commercial Distribution Discontinuation: 2021-11-01
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: M0064101010
• 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: 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

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729005278 [Primary]

FDA Product Code

• GBO: CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY

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: 2024-10-04
• Device Publish Date: 2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 08714729011378 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729011392 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729012580 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729012603 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729012610 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729056645 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729057062 - Lubriglide: 2024-12-23 Coated Guidewire
• 08714729080602 - MaxForce TTS: 2024-12-23 High Performance Balloon Dilatation Catheter