Clovis Vincent Spatula 07-959-13

GUDID 04946329402520

Clovis Vincent Spatula C Stainless

MIZUHO CORPORATION

Neurosurgical retraction system, brain
Primary Device ID04946329402520
NIH Device Record Key5bf6812a-3f5e-416d-90dd-846703786079
Commercial Distribution StatusIn Commercial Distribution
Brand NameClovis Vincent Spatula
Version Model Number07-959-13
Catalog Number07-959-13
Company DUNS690677802
Company NameMIZUHO CORPORATION
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

Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp
Phone9999999999
Emailregulatory@mizuho.co.jp

Device Dimensions

Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter
Length185 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104946329402520 [Primary]

FDA Product Code

HAOInstrument, Surgical, Non-Powered

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


[04946329402520]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-29
Device Publish Date2024-08-21

On-Brand Devices [Clovis Vincent Spatula]

04946329402520Clovis Vincent Spatula C Stainless
04946329402513Clovis Vincent Spatula B Stainless
04946329402506Clovis Vincent Spatula A Stainless

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