EXEL 1ml Syringe 25Gx1" LDS 26056

GUDID 10020221260561

EXEL 1ml Syringe 25Gx1" LDS, SINGLE UNIT BLISTERS, 100/BOX, 2,000/CS

Exel International

General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle General-purpose syringe/needle
Primary Device ID10020221260561
NIH Device Record Keycfdbf63d-dd25-4516-8eb8-ddfcedb7510e
Commercial Distribution StatusIn Commercial Distribution
Brand NameEXEL 1ml Syringe 25Gx1" LDS
Version Model Number26056
Catalog Number26056
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100020221260564 [Primary]
GS110020221260561 [Package]
Contains: 00020221260564
Package: Inner box [100 Units]
In Commercial Distribution
GS120020221260568 [Package]
Package: Outer box [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMFSyringe, Piston

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-23
Device Publish Date2023-03-15

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