ARMSTRONG X VENT TUBE

GUDID 00844505008501

Tympanostomy tube

Primary Device ID	00844505008501
NIH Device Record Key	8497a145-933c-486b-92e5-b73b180f85f3
Commercial Distribution Status	In Commercial Distribution
Brand Name	ARMSTRONG X VENT TUBE
Version Model Number	525-203
Company DUNS	030849173
Company Name	Grace Medical, Inc.
Device Count	1
DM Exempt	true
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 Issuing Agency	Device ID
GS1	00844505008501 [Primary]
GS1	10844505008508 [Package] Package: [30 Units] In Commercial Distribution

ETD	TUBE, TYMPANOSTOMY

Steralize Prior To Use	false
Device Is Sterile	true

00844505008501	ARMSTRONG X BEVELED GROMMET 1.14MM ID BLUE FLUOROPLASTIC 30 PACK
00844505008495	ARMSTRONG X BEVELED GROMMET 1.14MM ID BLUE FLUOROPLASTIC 5 PACK