GUDID 00385640000512

SUMMIT MEDICAL, INC.

Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use
Primary Device ID00385640000512
NIH Device Record Key4945fe2a-14f0-4046-988e-8c57e5ef1708
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberVA-1100
Company DUNS965484699
Company NameSUMMIT MEDICAL, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com
Phone888-229-2875
Emailcustomerservice@summitmedicalusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100385640000512 [Primary]
GS110385640000519 [Package]
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

JZFTube, Ear Suction

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-02-21
Device Publish Date2016-09-12

Devices Manufactured by SUMMIT MEDICAL, INC.

00385640081023 - INSTRUSAFE2024-05-20
00385640081009 - INSTRUSAFE2024-05-15
00385640081016 - INSTRUSAFE2024-05-15
00385640080996 - INSTRUSAFE2024-05-14
00385640080972 - INSTRUSAFE2024-05-13
00385640080989 - INSTRUSAFE2024-05-13
00385640080958 - INSTRUSAFE2024-05-08
00385640080965 - INSTRUSAFE2024-05-08
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.