ARMSTRONG VENT TUBE

GUDID 10844505014189

Tympanostomy tube

Primary Device ID	10844505014189
NIH Device Record Key	797620bf-6deb-442e-a0ff-ed4c52e83935
Commercial Distribution Status	In Commercial Distribution
Brand Name	ARMSTRONG VENT TUBE
Version Model Number	525-503
Company DUNS	030849173
Company Name	Grace Medical, Inc.
Device Count	1
DM Exempt	true
Pre-market Exempt	false
MRI Safety Status	MR Safe
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	00844505014182 [Primary]
GS1	10844505014189 [Package] Contains: 00844505014182 Package: [30 Units] In Commercial Distribution

ETD	Tube, Tympanostomy

Steralize Prior To Use	false
Device Is Sterile	true

10844505014271	ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 60 PACK
10844505014240	ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 60 PACK
10844505014189	ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 30 PACK
10844505014165	ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 30 PACK
10108445050141	ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 10 PACK
10844505014080	ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 10 PACK
10844505014042	ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 5 PACK
10844505014004	ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 5 PACK