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Mrs

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
MRS FDA UDI
Generic Name
Coated shoulder humeral stem prosthesis FDA UDI
Device Name
Humeral Module FDA UDI
Model / Reference
6487-2-075 FDA UDI
Description
Humeral Module FDA UDI

Identifiers

Catalog Number
6487-2-075 FDA UDI
Primary DI / UDI-DI
07613327049008 FDA UDI
510(k) Number
K954559 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Coated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 75.0 Millimeter FDA UDI

Category: Coated shoulder humeral stem prosthesis

Mrs by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated shoulder humeral stem prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8ad76e63-f34b-4b4e-b4b2-4eac1ed96ffe 36 fields · synced May 30, 2026