ARMSTRONG BEVELED GROMMET PACIFIC 114 MM ID FLUOROPLASTICPC COATED

GUDID 00821925039698

Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear while creating an avenue passage for air pressure equalization on either side of the drum.

Gyrus Acmi, Inc.

Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube
Primary Device ID00821925039698
NIH Device Record Key6f2a61e6-8138-48e9-830f-e48e2d3e2adf
Commercial Distribution StatusIn Commercial Distribution
Brand NameARMSTRONG BEVELED GROMMET PACIFIC 114 MM ID FLUOROPLASTICPC COATED
Version Model Number70146067
Company DUNS007198742
Company NameGyrus Acmi, Inc.
Device Count2
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx
Phone18002623540
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925021013 [Package]
Package: [60 Units]
In Commercial Distribution
GS100821925039698 [Primary]
GS100821925040762 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETDTube, Tympanostomy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [ARMSTRONG BEVELED GROMMET PACIFIC 114 MM ID FLUOROPLASTICPC COATED]

00821925039698Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi
00821925025424Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi

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