← Back to catalogue

Promos

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
PROMOS FDA UDI
Generic Name
Total shoulder prosthesis FDA UDI
Device Name
PROMOS HUMERAL STEM 5 NON-CEM FDA UDI
Model / Reference
75010867 FDA UDI
Description
PROMOS HUMERAL STEM 5 NON-CEM FDA UDI

Identifiers

Catalog Number
75010867 FDA UDI
Primary DI / UDI-DI
07611996037616 FDA UDI
510(k) Number
K081016 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Total shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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: Total shoulder prosthesis

Promos by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total shoulder prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5f58b323-9d81-4e0f-83a9-e75c3729bdaf 36 fields · synced Jun 8, 2026