AccessGUDID - DEVICE: Curve Hero™ (D848CURVEHERO0)

GUDID

Device Identifier (DI) Information

Brand Name: Curve Hero™
Version or Model: CURVE-HERO-I
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Curve Dental Ltd

Primary DI Number: D848CURVEHERO0
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 202952487 *Terms of Use

Device Description: Curve Dental® develops and markets a cloud-based dental practice management system titled Curve Hero™. Using a Mac or PC platform, a dental practice can use Curve Hero™ to manage all aspects of their practice, from scheduling to charting to billing, or from front desk to operatory. The application provides for secure and redundant management of all patient records and patient communications. Additionally, when utilizing Curve Dental’s® Curve Image™, the practice can also capture digital images directly to the cloud.

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?
40943	Radiology picture archiving and communication system workstation	A freestanding, image processing device that is a component of a picture archiving and communication system (PACS) for radiology designed to be networked with a wide variety of diagnostic imaging systems [e.g., x-ray, nuclear medicine, magnetic resonance imaging (MRI) or ultrasound (US), as well as a laboratory or hospital information system (HIS)]. It does not contain controls for the direct operation of a diagnostic imaging system and is designed to receive, archive, and transmit data both on-line and off-line. It is configured to provide limited or extensive capabilities to further process, manipulate and/or view patient images and information collected from diagnostic imaging systems.	Active	false

FDA Product Code

[?]

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

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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: 4f098fce-dfd1-4d1a-bc75-fcfce9ba332c
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: April 10, 2017