AccessGUDID - DEVICE: TiMO™ Tube Management Holder (19555240400083)

GUDID

Device Identifier (DI) Information

Brand Name: TiMO™ Tube Management Holder
Version or Model: C100400
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: ITL ASIA PACIFIC SDN. BHD.

Primary DI Number: 19555240400083
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1500
Labeler D-U-N-S® Number*: 597723837 *Terms of Use

Device Description: TiMO™ is intended as a sample test tube holder to assist with the management of the sample tubes during blood collection.

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:	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?
62011	Instrument/analyser specimen/reagent container carrier IVD	A device intended to hold a specimen/reagent container (e.g., test tube, tissue specimen petri dish, microplate, cuvette) on board an in vitro diagnostic laboratory instrument or analyser (e.g., PCR machine, spectrophotometric plate reader, biopsy specimen analyser, automated liquid handling station). It may be in the form of a removable tray (excludes immunoassay vehicle trays), holder, shuttle, rack/rack base, slotted case, or other format suitable to be handled and loaded into the parent device by the operator or via an automated process. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

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: 4a7d8566-a7e1-4d56-b3b4-94022873e764
Public Version Date: June 10, 2022
Public Version Number: 2
DI Record Publish Date: June 18, 2021