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Reflection

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
REFLECTION FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
REFLECTION XLPE 32MM INNER DIAMETER 20 DEGREE 66-68MM OUTER DIAMETER SIZE J FDA UDI
Model / Reference
71333338 FDA UDI
Description
REFLECTION XLPE 32MM INNER DIAMETER 20 DEGREE 66-68MM OUTER DIAMETER SIZE J FDA UDI

Identifiers

Catalog Number
71333338 FDA UDI
Primary DI / UDI-DI
03596010455710 FDA UDI
510(k) Number
K002747 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II 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

Category: Non-constrained polyethylene acetabular liner

Reflection 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 2b4a0faa-e033-4be9-97be-f2cf0d8f0b85 36 fields · synced Jun 8, 2026