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Emphasys

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
EMPHASYS FDA UDI
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Device Name
EMPHASYS TRIAL SHELL 60mm FDA UDI
Model / Reference
4810-60-900 FDA UDI
Description
EMPHASYS TRIAL SHELL 60mm FDA UDI

Identifiers

Catalog Number
481060900 FDA UDI
Primary DI / UDI-DI
10603295503873 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabulum prosthesis trial, prefabricated, reusable

Emphasys by Depuy (ireland) — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabulum prosthesis trial, prefabricated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 7450ab71-1d0c-4c94-8366-a993e4251cdd 35 fields · synced Jun 8, 2026