PowerPumpTM dp System Power Pump dp HP Interface B

GUDID 17350021986327

Medical Vision AB

Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable

• Primary Device ID: 17350021986327
• NIH Device Record Key: b9b37d24-1742-4e0c-8269-1a29ba0a4461
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerPumpTM dp System Power Pump dp HP Interface B
• Version Model Number: 941038G
• Company DUNS: 508778565
• Company Name: Medical Vision AB
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	17350021986327 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093409

FDA Product Code

• HRX: Arthroscope

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [PowerPumpTM dp System Power Pump dp HP Interface B]

• 17350021986747: 941025G
• 17350021986730: 941023G
• 17350021986709: 941015G
• 17350021986327: 941038G