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SMR TT Augmented 360

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR TT Augmented 360 FDA UDI
Generic Name
Shoulder glenoid fossa prosthesis, prefabricated FDA UDI
Device Name
SMR TT Augmented 360 Baseplate S-R +4mm, Dia. 27 mm FDA UDI
Model / Reference
1375.15.524 FDA UDI
Description
SMR TT Augmented 360 Baseplate S-R +4mm, Dia. 27 mm FDA UDI

Identifiers

Catalog Number
1375.15.524 FDA UDI
Primary DI / UDI-DI
08033390162104 FDA UDI
FDA Product Code
PHX FDA UDI
KWT FDA UDI
KWS FDA UDI
MBF FDA UDI
GMDN Term
Shoulder glenoid fossa prosthesis, prefabricated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3650 FDA UDI
888.3670 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Shoulder glenoid fossa prosthesis, prefabricated

SMR TT Augmented 360 by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoulder glenoid fossa prosthesis, prefabricated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 39a5b75a-e009-4130-a8cd-dd3c5a3ccad4 35 fields · synced May 30, 2026