AccessGUDID - DEVICE: ProPlan CMF (E314PROPLANCMFCONNECT0)

GUDID

Device Identifier (DI) Information

Brand Name: ProPlan CMF
Version or Model: ProPlan CMF Connect
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: ProPlan CMF Connect
Company Name: Materialise NV

Primary DI Number: E314PROPLANCMFCONNECT0
Issuing Agency: HIBCC
Commercial Distribution End Date: November 17, 2018
Device Count: 1
Labeler D-U-N-S® Number*: 373139427 *Terms of Use

Device Description: ProPlan CMF Connect

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
50484	CAD/CAM software	A software program intended to provide computer-aided design (CAD) or computer-aided manufacturing (CAM) functionality for the production of patient-specific custom-made devices (e.g., orthopaedic implants, dental devices, anatomical models), treatment planning, simulation, and/or robotic capabilities for device production (e.g., 3-D printing). It may include functionality to upload patient-specific images and to facilitate communication between healthcare professionals.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LLZ	System, Image Processing, Radiological

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K073449	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 02611e61-d5e9-40e5-a321-efa2b2293e09
Public Version Date: February 21, 2022
Public Version Number: 5
DI Record Publish Date: February 10, 2017