TROPHYscope

GUDID 04048551346396

TROPHY Curette

Karl Storz GmbH & Co. KG

Surgical/emergency suction cannula, non-illuminating, reusable

• Primary Device ID: 04048551346396
• NIH Device Record Key: 4a332328-8761-44c0-a132-fa81558ff658
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TROPHYscope
• Version Model Number: 26152DS
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	04048551346396 [Primary]

FDA Product Code

• NWW: Hysteroscope accessories

Sterilization

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

[04048551346396]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-20
• Device Publish Date: 2019-03-13

On-Brand Devices [TROPHYscope]

• 04048551276006: CAMPO TROPHYSCOPE®
• 04048551346396: TROPHY Curette
• 04048551261972: Continuous-Flow Operating Sheath
• 04048551258262: Continuous-Flow Operating Sheath