AccessGUDID - DEVICE: Reichert® 7CR Auto Tonometer (00812559011020)

GUDID

Device Identifier (DI) Information

Brand Name: Reichert® 7CR Auto Tonometer
Version or Model: 16060
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: REICHERT, INC.

Primary DI Number: 00812559011020
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 126650253 *Terms of Use

Device Description: AC -powered non-contact tonometer intended to measure the intraocular pressure of the eye, taking into consideration the biomechanical response of the cornea. An air puff is used to momentarily flatten a patient's cornea during the measurement.

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?
67414	Ophthalmic tonometer, professional	An ophthalmic, electrically-powered device intended to be used by a healthcare professional to measure intraocular pressure (IOP) by exerting an external force against the eye, which provides a reading of the resistance of the tunica of the eye to deformation (the extent of corneal indentation), typically for the diagnosis of glaucoma. It may have a light contact with the eye, have a bench-top or hand-held design, and use various techniques (e.g., the air-puff tonometer records deflections of the cornea from a puff of pressurized air).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HKX	Tonometer, Ac-Powered

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K081756	000

Device Exempt from Premarket Submission: No 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: 23467865-52b2-4777-b96e-7eb6a4453f53
Public Version Date: August 12, 2025
Public Version Number: 4
DI Record Publish Date: September 22, 2016