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Anthology

FDA UDI

Class III (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ANTHOLOGY FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 7 FDA UDI
Model / Reference
71357007 FDA UDI
Description
ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 7 FDA UDI

Identifiers

Catalog Number
71357007 FDA UDI
Primary DI / UDI-DI
03596010559500 FDA UDI
FDA Product Code
MRA FDA UDI
JDI FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Coated hip femur prosthesis, modularCoated femoral stem prosthesis, modular

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

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d080bd5-5064-4aac-8615-a888acfc77b3 35 fields · synced Jun 8, 2026