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SurgiCase Planner

FDA UDI

Class II (US FDA UDI)

by Materialise NV

Identity

Trade Name
SurgiCase Planner FDA UDI
Generic Name
CAD/CAM software FDA UDI
Device Name
SurgiCase Shoulder Planner FDA UDI
Model / Reference
SurgiCase Shoulder Planner FDA UDI
Description
SurgiCase Shoulder Planner FDA UDI

Identifiers

Catalog Number
SurgiCase Shoulder Planner FDA UDI
Primary DI / UDI-DI
E314SURGICASESHOULPLAN0 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
CAD/CAM software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: CAD/CAM software

SurgiCase Planner by Materialise NV — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CAD/CAM software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Materialise NV

Sources (1)

  • FDA UDI d48e7acb-3014-4fda-8559-38ef63c6f95f 34 fields · synced May 30, 2026