Geistlich Derma-Gide™

GUDID 07610221013203

Geistlich Pharma AG

Collagen wound matrix dressing
Primary Device ID07610221013203
NIH Device Record Key0be327fd-60c3-4d9d-b687-a6040b8fc6dd
Commercial Distribution StatusIn Commercial Distribution
Brand NameGeistlich Derma-Gide™
Version Model Number500478
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

Outer Diameter14 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107610221013203 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KGNDressing, Wound, Collagen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-05-06
Device Publish Date2019-01-31

On-Brand Devices [Geistlich Derma-Gide™]

07610221013227500480
07610221013210500479
07610221013203500478
07610221013197500477
07610221013180500476
07610221013173500475
07610221013166500474
07610221012626500427
07610221012619500426
07610221012602500425

Trademark Results [Geistlich Derma-Gide]

Mark Image

Registration | Serial
Company
Trademark
Application Date
GEISTLICH DERMA-GIDE
GEISTLICH DERMA-GIDE
87778500 5555339 Live/Registered
Geistlich Pharma AG
2018-01-31

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