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SMR Shoulder

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR Shoulder FDA UDI
Generic Name
Reverse shoulder prosthesis body FDA UDI
Device Name
SMR Shoulder - 140° Humeral Body Reverse FDA UDI
Model / Reference
1352.15.011 FDA UDI
Description
SMR Shoulder - 140° Humeral Body Reverse FDA UDI

Identifiers

Catalog Number
1352.15.011 FDA UDI
Primary DI / UDI-DI
08033390268233 FDA UDI
FDA Product Code
KWT FDA UDI
PHX FDA UDI
HSD FDA UDI
MBF FDA UDI
KWS FDA UDI
GMDN Term
Reverse shoulder prosthesis body FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3660 FDA UDI
888.3690 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: Reverse shoulder prosthesis body

SMR Shoulder by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse shoulder prosthesis body.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 144acf4f-0b1b-4444-aa00-6aec2de27903 35 fields · synced Jun 8, 2026