AccessGUDID - DEVICE: IMMUNO-TROL (03760170782102)

GUDID

Device Identifier (DI) Information

Brand Name: IMMUNO-TROL
Version or Model: GASTRITIS
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HM 068US-2X05
Company Name: THERADIAG SA

Primary DI Number: 03760170782102
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 391123478 *Terms of Use

Device Description: Reagent, prepared from human serum, intended for use as an unassayed precision control for determination of the following autoantibodies: anti-gastric parietal cells PCA, anti-intrinsic factor IF .

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):	No
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?
55079	Intrinsic factor/parietal cell antibody IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of antibodies to intrinsic factor and/or parietal cells in a clinical specimen.	Active	false
54989	Intrinsic factor antibody IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of antibodies to intrinsic factor in a clinical specimen.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
No Product Codes

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: 13319118-644c-4620-8aa7-58b4514a873a
Public Version Date: June 08, 2021
Public Version Number: 2
DI Record Publish Date: September 24, 2018