Wound Matrix PLUS

GUDID 07610221071913

Geistlich Pharma AG

Collagen wound matrix dressing

Primary Device ID	07610221071913
NIH Device Record Key	fd25c8c6-8c73-42d7-9f18-3c6954307477
Commercial Distribution Status	In Commercial Distribution
Brand Name	Wound Matrix PLUS
Version Model Number	501058
Company DUNS	480781728
Company Name	Geistlich Pharma AG
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter
Width	20 Millimeter
Height	40 Millimeter
Depth	6 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221071913 [Primary]

FDA Product Code

KGN	Dressing, Wound, Collagen

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2022-09-19
Device Publish Date	2022-09-09

On-Brand Devices [Wound Matrix PLUS]

07610221071913	501058
07610221071906	501057

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