Geistlich Nexo-Gide®

GUDID 07610221014217

Geistlich Pharma AG

Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer Tendon spacer

Primary Device ID	07610221014217
NIH Device Record Key	9e4941db-4586-4035-8ab2-cc73a58138a9
Commercial Distribution Status	In Commercial Distribution
Brand Name	Geistlich Nexo-Gide®
Version Model Number	500663
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	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter
Width	30 Millimeter
Height	40 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07610221014217 [Primary]

FDA Product Code

FTM	Mesh, Surgical

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	2021-09-09
Device Publish Date	2021-09-01

On-Brand Devices [Geistlich Nexo-Gide®]

07610221014224	500664
07610221014217	500663
07610221014200	500662