EXEL Spinal Needle 26970

GUDID 20020221269707

Spinal Needle, 25G x 3 1/2, QUINCKE BEVEL

Exel International

Spinal needle, single-use
Primary Device ID20020221269707
NIH Device Record Key67cbd0bc-eddd-42f9-80b1-50b85b047ac6
Commercial Distribution StatusIn Commercial Distribution
Brand NameEXEL Spinal Needle
Version Model Number26970
Catalog Number26970
Company DUNS180572216
Company NameExel International
Device Count50
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100020221269703 [Unit of Use]
GS110020221269700 [Primary]
GS120020221269707 [Package]
Contains: 10020221269700
Package: [2 Units]
In Commercial Distribution
GS130020221269704 [Package]
Package: Shipping carton [4 Units]
In Commercial Distribution
GS140020221269701 [Package]
Contains: 10020221269700
Package: Shipping carton [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

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 Number3
Public Version Date2023-04-20
Device Publish Date2016-09-23

On-Brand Devices [EXEL Spinal Needle]

20020221269653Spinal Needle, 22G x 2 3/4, QUINCKE BEVEL
20020221269707Spinal Needle, 25G x 3 1/2, QUINCKE BEVEL
20020221269677Spinal Needle, 22G x 3 1/2, QUINCKE BEVEL
20020221269646Spinal Needle, 20G x 3 1/2, QUINCKE BEVEL
10020221269601Spinal Needle, 18G x 3 1/2, QUINCKE BEVEL
20020221269615Spinal Needle, 20G x 2-3/4, QUINCKE BEVEL

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.