Harper Brush,(2xEnd),Sterile,

GUDID 00840113209828

Intended to remove surgical residue from surgical instruments and endoscopic devices after surgical procedures

ASPEN SURGICAL PRODUCTS, INC.

Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning brush/tool, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use Surgical instrument/endoscope cleaning utensil, single-use
Primary Device ID00840113209828
NIH Device Record Keyb6c5b92e-44c4-41ae-af86-808d44f0de62
Commercial Distribution StatusIn Commercial Distribution
Brand NameHarper Brush,(2xEnd),Sterile,
Version Model Number243014PBXHAR
Company DUNS027680821
Company NameASPEN SURGICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com
Phone+1(616)698-7100
Emailcustomerservice@aspensurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840113209828 [Package]
Contains: 00840113209835
Package: [12 Units]
In Commercial Distribution
GS100840113209835 [Primary]

FDA Product Code

MNLACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-05
Device Publish Date2021-03-28

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00840113231584 - PlastiBell Circumcision Device2023-03-07 1.4 cm PlastiBell Circumcision Device
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