EXEL BLUNT TIP ALUMINUM STERILE HUB NEEDLE 26475

GUDID 30020221264754

Needle, 20G X 1 1/2"; 25/BOX, 100/CASE, 10CS/CRTN

Exel International

Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose
Primary Device ID30020221264754
NIH Device Record Key99c41765-eecc-410e-af24-4ab8d9acacb3
Commercial Distribution StatusIn Commercial Distribution
Brand NameEXEL BLUNT TIP ALUMINUM STERILE HUB NEEDLE
Version Model Number26475
Catalog Number26475
Company DUNS180572216
Company NameExel International
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

Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com
Phone8009403935
Emailinfo@exelint.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100020221264753 [Primary]
GS110020221264750 [Package]
Contains: 00020221264753
Package: Box [25 Units]
In Commercial Distribution
GS120020221264757 [Package]
Contains: 10020221264750
Package: Case [4 Units]
In Commercial Distribution
GS130020221264754 [Package]
Contains: 20020221264757
Package: Carton [10 Units]
In Commercial Distribution
GS140020221264751 [Package]
Package: Export carton [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LHISet, I.V. Fluid Transfer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-07-24
Device Publish Date2019-07-16

On-Brand Devices [EXEL BLUNT TIP ALUMINUM STERILE HUB NEEDLE]

30020221264723Needle, 17G X 1 1/2"; 25/BOX, 100/CASE, 10CS/CRTN
30020221264716Needle, 15G x 1 1/2" 25/BOX, 100/CASE, 10CS/CRTN
30020221264754Needle, 20G X 1 1/2"; 25/BOX, 100/CASE, 10CS/CRTN
30020221264747Needle, 19G X 1 1/2"; 25 PCS/BOX, 100 PCS/CASE, 10CS/CRTN
30020221264730Needle, 18G X 1"; 25/BOX, 100/CASE, 10CS/CRTN
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.