DEFENDO Air/Water/Suction and Biopsy Valve

GUDID 00677964060250

MEDIVATORS INC.

Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit Endoscope channel support kit

• Primary Device ID: 00677964060250
• NIH Device Record Key: 83b4a175-c52b-44b8-a16c-75fe1902272c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DEFENDO Air/Water/Suction and Biopsy Valve
• Version Model Number: 100305
• Company DUNS: 068199363
• Company Name: MEDIVATORS INC.
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00677964060250 [Primary]
GS1	10677964060257 [Package]; Package: Carton [50 Units]; In Commercial Distribution
GS1	20677964060254 [Package]; Package: Case [100 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090851

FDA Product Code

• ODC: Endoscope Channel Accessory

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: 2018-08-15
• Device Publish Date: 2016-09-21

On-Brand Devices [DEFENDO Air/Water/Suction and Biopsy Valve]

• 00677964060250: 100305
• 00677964055928: 100316