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Nexus

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
Nexus FDA UDI
Generic Name
Orthopaedic cement spacer FDA UDI
Device Name
DISTAL CEMENT SPACER SZ 12 FDA UDI
Model / Reference
20020112 FDA UDI
Description
DISTAL CEMENT SPACER SZ 12 FDA UDI

Identifiers

Catalog Number
20020112 FDA UDI
Primary DI / UDI-DI
M684200201121 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Orthopaedic cement spacer 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

No

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

Category: Orthopaedic cement spacer

Nexus by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement spacer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d5c97880-1242-4f5b-a176-e2813eaa34ee 35 fields · synced Jun 9, 2026