Geistlich Bio-Gide®

GUDID 07610221014309

Geistlich Pharma AG

Collagen dental regeneration membrane
Primary Device ID07610221014309
NIH Device Record Key6e657e32-7ce8-4c13-a495-41bfd2aa9740
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeistlich Bio-Gide®
Version Model Number500710
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

Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter
Width30 Millimeter
Height40 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107610221014309 [Primary]

FDA Product Code

NPLBarrier, Animal Source, Intraoral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-09
Device Publish Date2020-12-01

On-Brand Devices [Geistlich Bio-Gide®]

0761022101042420153
0761022101041720152
0761022101040020151
07610221014309500710

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