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Gmrs

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
GMRS FDA UDI
Generic Name
Uncoated hip femur prosthesis, modular FDA UDI
Device Name
Extension Piece FDA UDI
Model / Reference
6495-6-140 FDA UDI
Description
Extension Piece FDA UDI

Identifiers

Catalog Number
6495-6-140 FDA UDI
Primary DI / UDI-DI
07613327049275 FDA UDI
510(k) Number
K023087 FDA UDI
K222056 FDA UDI
FDA Product Code
KRO FDA UDI
JDI FDA UDI
GMDN Term
Uncoated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3510 FDA UDI
888.3350 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
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 140.0 Millimeter FDA UDI

Category: Uncoated hip femur prosthesis, modular

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

Similar devices

Also classified as Uncoated hip femur prosthesis, modular.

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 3fa30467-dcdb-473f-a357-124114eeef66 36 fields · synced May 30, 2026