NIPRO SafeTouch™ Safety Scalp Vein Set

GUDID 10383790002599

NIPRO MEDICAL CORPORATION

Scalp vein needle
Primary Device ID10383790002599
NIH Device Record Key0014d9f2-d7f3-4748-a6fe-72c436cb1964
Commercial Distribution StatusIn Commercial Distribution
Brand NameNIPRO SafeTouch™ Safety Scalp Vein Set
Version Model NumberSPR+21G19
Company DUNS797372554
Company NameNIPRO MEDICAL 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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 (908) 393-7030
Emailinfo@nipromed.com
Phone+1 (908) 393-7030
Emailinfo@nipromed.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100383790002592 [Primary]
GS110383790002599 [Package]
Contains: 00383790002592
Package: [50 Units]
In Commercial Distribution
GS140383790002590 [Package]
Package: [10 Units]
In Commercial Distribution

FDA Product Code

FMINeedle, hypodermic, single lumen

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 [NIPRO SafeTouch™ Safety Scalp Vein Set]

40383790002613SPR+25G19
10383790002605SPR+23G19
10383790002599SPR+21G19
40383790002583SPR+19G19

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