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Contour

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Contour FDA UDI
Generic Name
Extra-gynaecological surgical mesh, metal FDA UDI
Device Name
CONTOUR ACETABULAR REINFORCEMENT RING 47MM OUTER DIAMETER 43MM INNER DIAMETER FDA UDI
Model / Reference
71337047 FDA UDI
Description
CONTOUR ACETABULAR REINFORCEMENT RING 47MM OUTER DIAMETER 43MM INNER DIAMETER FDA UDI

Identifiers

Catalog Number
71337047 FDA UDI
Primary DI / UDI-DI
03596010293299 FDA UDI
510(k) Number
K211176 FDA UDI
K962541 FDA UDI
FDA Product Code
JDJ FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, metal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Extra-gynaecological surgical mesh, metal

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

Similar devices

Also classified as Extra-gynaecological surgical mesh, metal.

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 e2bec0d3-cb17-43b9-b374-7c9153bc7069 37 fields · synced Jun 8, 2026