AccessGUDID - DEVICE: TIMS System (00850951007272)

GUDID

Device Identifier (DI) Information

Brand Name: TIMS System
Version or Model: TIMS OEM Rev L
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 061000-OEM-CPU-HD+C
Company Name: FORESIGHT IMAGING, LLC

Primary DI Number: 00850951007272
Issuing Agency: GS1
Commercial Distribution End Date: May 09, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 144124518 *Terms of Use

Device Description: TIMS System connects to all analog and digital modalities. Usage includes video and image acquisition, CD/DVD/USB burning.

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 [?]
K001947	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: 3b782785-f130-4e69-9b79-2e40219cfa8c
Public Version Date: May 12, 2025
Public Version Number: 2
DI Record Publish Date: April 12, 2019