AccessGUDID - DEVICE: KIRO Link (08437014572308)

GUDID

Device Identifier (DI) Information

Brand Name: KIRO Link
Version or Model: 1006
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: KIRO GRIFOLS SL.

Primary DI Number: 08437014572308
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 464246224 *Terms of Use

Device Description: KIRO Link is a software intended to enter, store, convert, transfer and display the data to support the integration and workflow management functionalities of Pharmacy Compounding Devices (PCDs) with customer site softwares such as Computerized Physician Order Entry (CPOE), logistics, quality control and compounding assisting software. KIRO Link is intended to be used only by qualified pharmacy personnel.

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?
63888	Medical equipment non-clinical data monitoring software	An application software program intended to extract, process, and store non-clinical processing data (e.g., log of equipment usage, equipment status) from medical equipment (e.g., sterilizers/disinfectors, refrigerators) to assist process management. It is not intended for control of equipment.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OUG	Medical Device Data System

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: f9aa368d-4ecb-4b08-8d7b-0c3f3ec04ace
Public Version Date: September 10, 2024
Public Version Number: 3
DI Record Publish Date: November 07, 2018