AccessGUDID - DEVICE: HD Analyzer (18437014903024)

GUDID

Device Identifier (DI) Information

Brand Name: HD Analyzer
Version or Model: .OQAS
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: .OQAS
Company Name: VISIOMETRICS SL

Primary DI Number: 18437014903024
Issuing Agency: GS1
Commercial Distribution End Date: July 13, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 465168057 *Terms of Use

Device Description: HD Analyzer Optical Quality Analysis System

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):	Yes
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?
36386	Automated ophthalmic refractometer	An electrically-powered, ophthalmic device designed to be used by a healthcare professional to objectively measure the refractive error of the eye (the inaccuracies of focusing light upon the retina) by measuring how light is changed when it enters the patient's eye(s). The device emits light into the eye and detects the light reflection which is measured for sphere, cylinder, axis and/or high order aberration measurements, typically measured in dioptres (the reciprocal of the focal length of the lens expressed in metres). Also known as an aberrometer, the device uses this information to automatically calculate the lens prescription needed to correct the patient's vision.	Active	false
62592	Meibomian gland camera	A mains electricity (AC-powered) optical device intended for infrared (IR) image capture of the meibomian glands for evaluation of structural abnormalities of the meibomian glands. It includes patient head/chin supports, an IR source(s), IR camera, controls and appropriate software intended to enable analysis of the images; it may include an eyelid everter to assist imaging of the meibomian glands.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NCF	Aberrometer, ophthalmic
PJZ	Camera, ophthalmic, general-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
Storage Environment Humidity: between 10 and 95 Percent (%) Relative Humidity
Storage Environment Temperature: between -10 and 55 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: eb837d68-6764-46f3-be32-d569174089dd
Public Version Date: April 11, 2024
Public Version Number: 3
DI Record Publish Date: January 21, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: Yes
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: Yes
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +34935824501
Email: technicalservice@visiometrics.com

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