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Durasul®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Durasul® FDA UDI
Generic Name
Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Model / Reference
4405-26-048 FDA UDI

Identifiers

Catalog Number
4405-26-048 FDA UDI
Primary DI / UDI-DI
00889024365766 FDA UDI
510(k) Number
K040947 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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

Dimensions & Sizes

Size
Lumen/Inner Diameter — 26 Millimeter FDA UDI

Category: Bipolar femoral head outer component, hemiarthroplasty

Durasul® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bipolar femoral head outer component, hemiarthroplasty.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 8e837a1f-f264-4792-96d5-f1bca93822d8 36 fields · synced Jun 6, 2026