SCANLAN® Instrumentation CDA003-09

GUDID 00846159035919

Suction Instrument

SCANLAN INTERNATIONAL INC

Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable
Primary Device ID00846159035919
NIH Device Record Key1e452152-db0e-4026-9bbf-e0c54b24838a
Commercial Distribution StatusIn Commercial Distribution
Brand NameSCANLAN® Instrumentation
Version Model NumberCDA003-09
Catalog NumberCDA003-09
Company DUNS023055619
Company NameSCANLAN INTERNATIONAL 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 Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com
Phone651-298-0997
Emailvanderpoelw@scanlangroup.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100846159035919 [Primary]

FDA Product Code

JOLCatheter And Tip, Suction

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


[00846159035919]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-07
Device Publish Date2023-03-30

On-Brand Devices [SCANLAN® Instrumentation]

00846159026801SCANLAN® Septal Hook
00846159026764SCANLAN® Septal Hook
00846159035643SCANLAN® Cardiovascular Probe
00846159033656Kerrison Style Wire Cutter
00846159035858SCANLAN® Retractor Blade
00846159035841SCANLAN® Retractor Blade
00846159035919Suction Instrument
00846159036046Miller™ Periosteal Elevator Curved
00846159036039Miller™ Periosteal Elevator Curved

Trademark Results [SCANLAN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SCANLAN
SCANLAN
74389302 1837794 Live/Registered
Scanlan International, Inc.
1993-05-07
SCANLAN
SCANLAN
73625084 1439873 Live/Registered
SCANLAN INTERNATIONAL, INC.
1986-10-14

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