Exeter

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name: Exeter FDA UDI
Generic Name: Polyethylene acetabulum prosthesis FDA UDI
Device Name: RimFit Cup FDA UDI
Model / Reference: 7309-2-240 FDA UDI
Description: RimFit Cup FDA UDI

Identifiers

Catalog Number: 7309-2-240 FDA UDI
Primary DI / UDI-DI: 07613327383911 FDA UDI
FDA Product Code: KWY FDA UDI
LZO FDA UDI
JDG FDA UDI
JDI FDA UDI
GMDN Term: Polyethylene acetabulum prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3390 FDA UDI
888.3353 FDA UDI
888.3360 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 22.2 Millimeter FDA UDI
Outer Diameter — 40.0 Millimeter FDA UDI

Category: Polyethylene acetabulum prosthesis

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

Similar devices

Also classified as Polyethylene acetabulum prosthesis.

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REFLECTION — Smith & Nephew, Inc. · Class II
ZCA® — Zimmer, Inc. · Class II
ONVOY — GLOBUS MEDICAL, INC. · Class II
Acetabular Cup — WALDEMAR LINK GmbH & Co. KG · Class II
ZCA® — Zimmer, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Howmedica Osteonics Corp.

Sources (1)

FDA UDI 83c196e9-373a-4825-90d8-8808bd9aeb84 35 fields · synced May 30, 2026