PNEUMOSTOP® 110230

GUDID 10850200006756

PNEUMOSTOP® PLUS DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® PLUS DEVICE.

LSI Solutions, Inc.

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Primary Device ID10850200006756
NIH Device Record Keyc9fc0a94-351e-4f6e-bd9d-a2749452c64a
Commercial Distribution StatusIn Commercial Distribution
Brand NamePNEUMOSTOP®
Version Model Number110230
Catalog Number110230
Company DUNS603420183
Company NameLSI Solutions, Inc.
Device Count3
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com
Phone+1(866)575-3493
Emailregulatorydpt@lsisolutions.com

Device Dimensions

Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100850200006759 [Primary]
GS110850200006756 [Package]
Contains: 00850200006759
Package: Inner pack [6 Units]
In Commercial Distribution
GS140850200006757 [Unit of Use]

FDA Product Code

NWWHysteroscope accessories

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


[10850200006756]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-13
Device Publish Date2020-07-03

On-Brand Devices [PNEUMOSTOP®]

10850200006756PNEUMOSTOP® PLUS DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® PLUS DE
10850200006749PNEUMOSTOP® DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® DEVICE.
10850012846014PNEUMOSTOP® PLUS DEVICE
10850012846007PNEUMOSTOP® DEVICE

Trademark Results [PNEUMOSTOP]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PNEUMOSTOP
PNEUMOSTOP
86024532 4598672 Live/Registered
LSI SOLUTIONS, INC.
2013-07-31
PNEUMOSTOP
PNEUMOSTOP
74173304 1691554 Live/Registered
BLOHM + VOSS INDUSTRIES GMBH
1991-06-06
PNEUMOSTOP
PNEUMOSTOP
73450042 1363355 Dead/Cancelled
HOWALDTSWERKE - DEUTSCHE WERFT
1983-10-27

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