DeSoutter

GUDID 00810041638243

Provision

Laparoscopic access cannula, reprocessed Laparoscopic access cannula, reprocessed Laparoscopic access cannula, reprocessed Laparoscopic access cannula, reprocessed
Primary Device ID00810041638243
NIH Device Record Keybc178862-11e0-4290-b339-a4723c1df69a
Commercial Distribution StatusIn Commercial Distribution
Brand NameDeSoutter
Version Model NumberS89-3656
Company DUNS016889401
Company NameProvision
Device Count1
DM Exempttrue
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 Datetrue
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
GS100810041638243 [Primary]
GS100810041638243 [Primary]
GS100810041638243 [Primary]
GS100810041638243 [Primary]

FDA Product Code

NBHAccessories, Arthroscopic
NBHAccessories, Arthroscopic
NBHAccessories, Arthroscopic
NBHAccessories, Arthroscopic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-21
Device Publish Date2020-05-13

On-Brand Devices [DeSoutter]

B504OMS8996560S89-9656
B504OMS8936560S89-3656
B504OMS8605340S86-0534
00810041638250S89-9656
00810041638243S89-3656
00810041638236S86-0534

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