A-V Impulse AV6000-GER

GUDID 10884521043923

6000 Series Controller

Cardinal Health, Inc.

Intermittent venous compression system
Primary Device ID10884521043923
NIH Device Record Key46a1d8ac-7c5c-47cd-b5ee-9b6395bbb86a
Commercial Distribution StatusIn Commercial Distribution
Brand NameA-V Impulse
Version Model NumberAV6000-GER
Catalog NumberAV6000-GER
Company DUNS080935429
Company NameCardinal Health, Inc.
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry;Fragile;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521043923 [Primary]

FDA Product Code

JOWSLEEVE, LIMB, COMPRESSIBLE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number7
Public Version Date2019-04-15
Device Publish Date2016-09-24

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