IceSeed™ H7493968333170

GUDID 00191506055752

Cryoablation Needle

BOSTON SCIENTIFIC CORPORATION

Cryosurgical set

• Primary Device ID: 00191506055752
• NIH Device Record Key: cdfccf3f-8c1e-4dcf-9d80-eb06fc6d9938
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IceSeed™
• Version Model Number: H7493968333170
• Catalog Number: H7493968333170
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge
• Length: 175 Millimeter
• Needle Gauge: 17 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00191506055752 [Primary]

FDA Product Code

• GEH: UNIT, CRYOSURGICAL, ACCESSORIES

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-27
• Device Publish Date: 2025-02-19

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• 08714729424222 - Contour™: 2026-02-17 Ureteral Stent Set