Geistlich Nexo-Gide®

GUDID 07610221014224

Geistlich Pharma AG

Tendon spacer
Primary Device ID07610221014224
NIH Device Record Key8a053bbc-807b-44a1-aa5e-f959e6c1b55b
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeistlich Nexo-Gide®
Version Model Number500664
Company DUNS480781728
Company NameGeistlich Pharma AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Device Dimensions

Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter
Width40 Millimeter
Height50 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107610221014224 [Primary]

FDA Product Code

FTMMesh, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-09
Device Publish Date2021-09-01

On-Brand Devices [Geistlich Nexo-Gide®]

07610221014224500664
07610221014217500663
07610221014200500662

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