AccessGUDID - DEVICE: Ca (05055273200911)

GUDID

Device Identifier (DI) Information

Brand Name: Ca
Version or Model: CA590
Commercial Distribution Status: In Commercial Distribution
Catalog Number: CA590
Company Name: RANDOX LABORATORIES LIMITED

Primary DI Number: 05055273200911
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 227530649 *Terms of Use

Device Description: The calcium test system is a device intended for the quantitative in vitro determination of calcium in serum, plasma or urine

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:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
52875	Calcium (Ca2+) IVD, reagent	A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the quantitative measurement of calcium (Ca2+) in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CIC	Cresolphthalein Complexone, Calcium

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K000375	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
Special Storage Condition, Specify: Stable for 7 days at +2 to +8°C or 3 days at +15 to +25°C once reconstituted.
Storage Environment Temperature: between 15 and 25 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e344f6bf-a8d0-4bbc-9315-4793d22745c8
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 16, 2016