Blade for Dermatome 50mm

GUDID ENOU19969

Blade for Dermatome 50mm

Nouvag AG

Dermatome blade, single-use
Primary Device IDENOU19969
NIH Device Record Key5c2f9774-aa67-4df7-8478-55d3916047ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameBlade for Dermatome 50mm
Version Model Number1996
Company DUNS480610476
Company NameNouvag AG
Device Count10
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCENOU19960 [Unit of Use]
HIBCCENOU19969 [Primary]

FDA Product Code

GFDDermatome

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-21
Device Publish Date2018-08-21

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