AccessGUDID - DEVICE: Acucy Calibration Device (00742860100345)

GUDID

Device Identifier (DI) Information

Brand Name: Acucy Calibration Device
Version or Model: 1031
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: SEKISUI DIAGNOSTICS, LLC

Primary DI Number: 00742860100345
Issuing Agency: GS1
Commercial Distribution End Date: September 24, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 966812344 *Terms of Use

Device Description: No description.

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):	Yes
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?
58049	Optical laboratory instrument performance standard calibrator/control IVD, reusable	A solid phase or liquid reference standard of known optical and physical characteristics intended to be used to verify and/or optimise the performance of an optical laboratory instrument (e.g., spectrophotometer, nephelometer, microplate reader). It is typically presented as a solid/sealed cuvette or a multiple-well test plate and may include filters or a light source emitted at specified wavelengths. Verification/optimization functions may include optical density (absorbance/scattering), fluorescent or luminescent accuracy, linearity, repeatability and/or limit of detection readings, and optical alignment and precision of the instrument/analyser. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PSZ	Devices Detecting Influenza A, B, And C Virus Antigens

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: 387cfaef-aa3e-454a-9492-d23d2a98031d
Public Version Date: December 20, 2022
Public Version Number: 4
DI Record Publish Date: September 24, 2019