NIPRO SCALP VEIN SET

GUDID 40383790002477

NIPRO MEDICAL CORPORATION

Scalp vein needle
Primary Device ID40383790002477
NIH Device Record Key203dd39b-1204-4423-bcf4-d026be1c3f3a
Commercial Distribution StatusIn Commercial Distribution
Brand NameNIPRO SCALP VEIN SET
Version Model NumberPR+19G19
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
GS100383790002479 [Primary]
GS110383790002476 [Package]
Contains: 00383790002479
Package: [50 Units]
In Commercial Distribution
GS140383790002477 [Package]
Contains: 10383790002476
Package: [20 Units]
In Commercial Distribution

FDA Product Code

FOZCatheter,intravascular,therapeutic,short-term less than 30 days

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 SCALP VEIN SET]

40383790002552PR+27G19
10383790002537PR+25G19
10383790002513PR+23G19
40383790002507PR+22G19
40383790002491PR+21G19
40383790002477PR+19G19
10383790002469PR+18G19

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