AccessGUDID - DEVICE: Vein Illuminator (06926802602812)

GUDID

Device Identifier (DI) Information

Brand Name: Vein Illuminator
Version or Model: NAVI-60
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MEDCAPTAIN MEDICAL TECHNOLOGY CO., LTD.

Primary DI Number: 06926802602812
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 543036737 *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?
48040	Infrared-light vein locator	A portable, hand-held, electrically-powered device designed to help locate peripheral veins beneath the skin (subcutaneous) using infrared (IR) laser-generated light. It is intended to illuminate the position of veins on the skin surface directly above the veins to assist a healthcare professional in finding a vein of the right size and position for venipuncture. It may also be known as an IR vein finder, viewer or transilluminator, and may include a small interface screen to cycle through previously stored display settings to help optimize vein display for the patient undergoing examination/treatment.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KZA	Device, Vein Location, Liquid Crystal

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: baef6ed8-524b-4469-8b20-0eb0df43f0ae
Public Version Date: February 13, 2024
Public Version Number: 1
DI Record Publish Date: February 05, 2024