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Smr Lateralized Connector

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR LATERALIZED CONNECTOR FDA UDI
Generic Name
Reverse shoulder prosthesis head FDA UDI
Device Name
Connector Lat +5 mm + Screw - SMALL-R FDA UDI
Model / Reference
1374.15.315 FDA UDI
Description
Connector Lat +5 mm + Screw - SMALL-R FDA UDI

Identifiers

Catalog Number
1374.15.315 FDA UDI
Primary DI / UDI-DI
08033390152129 FDA UDI
510(k) Number
K183042 FDA UDI
FDA Product Code
PHX FDA UDI
MBF FDA UDI
KWT FDA UDI
KWS FDA UDI
GMDN Term
Reverse shoulder prosthesis head FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3670 FDA UDI
888.3650 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 head

Smr Lateralized Connector by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reverse shoulder prosthesis head.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI a68dfe92-fe5e-4921-8802-4afd4d92ac57 36 fields · synced May 30, 2026