AccessGUDID - DEVICE: Plasma Control (04250317544322)

GUDID

Device Identifier (DI) Information

Brand Name: Plasma Control
Version or Model: 0132
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 0132
Company Name: Chromsystems Instruments + Chemicals GmbH

Primary DI Number: 04250317544322
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 328712260 *Terms of Use

Device Description: Plasma Control Level I Perazine, Quetiapine, Citalopram

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?
65020	Multiple antipsychotic therapeutic drug monitoring IVD, control	A material which is used to verify the performance of an assay intended to be used for the quantitative measurement and therapeutic monitoring of multiple antipsychotic drugs, also known as neuroleptic drugs which may include amisulpride, chlorprothixene, melperone and ziprazidone, in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LAS	Drug Specific Control Materials

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
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 10 x 5ml

Device Record Status

Public Device Record Key: 5ea17393-ad90-45eb-9e37-8fd3bd7dce52
Public Version Date: September 04, 2020
Public Version Number: 1
DI Record Publish Date: August 27, 2020