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R3

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
R3 FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
R3 0 DEGREE XLPE ACETABULAR LINER 36MM X 66/70MM OUTER DIAMETER FDA UDI
Model / Reference
71330766 FDA UDI
Description
R3 0 DEGREE XLPE ACETABULAR LINER 36MM X 66/70MM OUTER DIAMETER FDA UDI

Identifiers

Catalog Number
71330766 FDA UDI
Primary DI / UDI-DI
00885556020296 FDA UDI
510(k) Number
K092386 FDA UDI
K211176 FDA UDI
FDA Product Code
MBL FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

Category: Non-constrained polyethylene acetabular liner

R3 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

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 f6bf1c23-99e9-43c7-bf33-a980730afca9 36 fields · synced Jun 8, 2026