Suction tip

GUDID 10803622105897

LIVANOVA USA, INC.

Surgical/emergency suction cannula, non-illuminating, single-use
Primary Device ID10803622105897
NIH Device Record Key7e6e41ad-2dc0-4c1d-8b30-431f03df2fb0
Commercial Distribution StatusIn Commercial Distribution
Brand NameSuction tip
Version Model NumberSU-xxxxx
Company DUNS080914995
Company NameLIVANOVA USA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100803622105890 [Primary]
GS110803622105897 [Package]
Contains: 00803622105890
Package: CASE [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTSSUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-02-21
Device Publish Date2015-07-16

On-Brand Devices [Suction tip]

10803622105910SU-xxxxx
10803622105903SU-xxxxx
10803622105897SU-xxxxx
10803622105880SU-xxxxx
10803622105873SU-xxxxx
10803622105866SU-xxxxx
10803622105859SU-xxxxx
10803622105842SU-xxxxx
10803622105835SU-xxxxx
10803622105828SU-xxxxx
10803622105811SU-xxxxx
10803622105804SU-xxxxx

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