Medisystems OneSite dual lumen buttonhole needle with steripick

GUDID 10842289100791

MEDISYSTEMS CORPORATION

Haemodialysis needle
Primary Device ID10842289100791
NIH Device Record Key19167579-8e82-4719-93b8-fe44a91cdc26
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedisystems OneSite dual lumen buttonhole needle with steripick
Version Model NumberDL-2014PE
Company DUNS061310132
Company NameMEDISYSTEMS CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-866-697-8243
Emailinfo@nxstage.com

Device Dimensions

Needle Gauge14 Gauge
Needle Gauge14 Gauge

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100842289100794 [Primary]
GS110842289100791 [Package]
Contains: 00842289100794
Package: [150 Units]
In Commercial Distribution

FDA Product Code

FIENeedle, Fistula

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-16

On-Brand Devices [Medisystems OneSite dual lumen buttonhole needle with steripick]

10842289100791DL-2014PE
10842289100777DL-2004PE
10842289100753DL-1214PE
10842289100739DL-1204PE

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