SMR TT Augmented 360 1375.15.519

GUDID 08033390161503

Shoulder glenoid fossa prosthesis, prefabricated

Primary Device ID	08033390161503
NIH Device Record Key	3370d567-5c6f-4342-b0a0-82e89bb94d50
Commercial Distribution Status	In Commercial Distribution
Brand Name	SMR TT Augmented 360
Version Model Number	1375.15.519
Catalog Number	1375.15.519
Company DUNS	432066322
Company Name	LIMACORPORATE SPA
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 Issuing Agency	Device ID
GS1	08033390161503 [Primary]

PHX	Shoulder Prosthesis, Reverse Configuration

Steralize Prior To Use	false
Device Is Sterile	true

08033390162104	SMR TT Augmented 360 Baseplate S-R +4mm, Dia. 27 mm
08033390161848	SMR TT Augmented 360 Baseplate S-R +2mm, Dia. 27 mm
08033390161473	SMR TT Augmented 360 Baseplate S-R 15°, Dia. 27 mm
08033390161466	SMR TT Augmented 360 Baseplate S-R 10°, Dia. 27 mm
08033390161459	SMR TT Augmented 360 Baseplate S-R 7°, Dia. 27 mm
08033390180337	SMR TT Augmented 360 Baseplate S-R 15°X
08033390180320	SMR TT Augmented 360 Baseplate S-R 10°X
08033390180313	SMR TT Augmented 360 Baseplate S-R 7°X
08033390180047	SMR TT Augmented 360 Baseplate S-R 19°X
08033390161503	SMR TT Augmented 360 Baseplate S-R 19°