ArtiFascia® ART7701

GUDID 07290019685029

ArtiFascia® is an absorbable dural repair graft for the repair of cranial dural defects. ArtiFascia® is a highly flexible, easy to handle, non-friable soft matrix composed of synthetic non-woven fibers and a non-porous film. ArtiFascia® readily conforms to the surface of the wound area and is applied to the dural defect by using sutures.

NURAMI MEDICAL LTD

Dura mater graft, synthetic
Primary Device ID07290019685029
NIH Device Record Key6f9c3b85-ff1f-4c2b-9de3-c9da7ed7230c
Commercial Distribution StatusIn Commercial Distribution
Brand NameArtiFascia®
Version Model Number7cm X 7cm (2.75" X 2.75")
Catalog NumberART7701
Company DUNS600262998
Company NameNURAMI MEDICAL LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com
Phone(610) 317-1670
Emailsupport@nurami-medical.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS107290019685029 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GXQDura Substitute

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-22
Device Publish Date2024-03-14

On-Brand Devices [ArtiFascia®]

07290019685029ArtiFascia® is an absorbable dural repair graft for the repair of cranial dural defects. ArtiFa
07290019685012ArtiFascia® is an absorbable dural repair graft for the repair of cranial dural defects. ArtiFa
07290019685005ArtiFascia® is an absorbable dural repair graft for the repair of cranial dural defects. ArtiFa

Trademark Results [ArtiFascia]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ARTIFASCIA
ARTIFASCIA
97587126 not registered Live/Pending
NURAMI MEDICAL Ltd.
2022-09-12

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.