PowerPumpTM dp System Interface Cable, Type 6

GUDID 17350021986792

Compatible with: Atlantech Revlt

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 ID17350021986792
NIH Device Record Keybda18393-0a9b-4edf-9291-fc0f4eb6a1b2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePowerPumpTM dp System Interface Cable, Type 6
Version Model Number941034G
Company DUNS508778565
Company NameMedical Vision AB
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS117350021986792 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

Devices Manufactured by Medical Vision AB

17350021987003 - PowerPumpTM dp System Day Cassette2019-04-23
17350021987027 - PowerPumpTM dp System Patient cassette2019-04-23
17350021987058 - PowerPumpTM dp System Patient tubing2019-04-23
07350021981202 - Double Pump Day cassette/ Double Pump RF Day cassette2019-04-23
07350021981523 - Double Pump Single/ Double Pump RF Single2019-04-23
07350021982209 - Double Pump Patient cassette2019-04-23
07350021982704 - Double Pump RF Patient cassette2019-04-23
17350021986105 - PowerPumpTM dp System2018-07-06

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