AccessGUDID - DEVICE: ESSILOR (03664188000558)

GUDID

Device Identifier (DI) Information

Brand Name: ESSILOR
Version or Model: WAM 700+
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: LUNEAU TECHNOLOGY OPERATIONS

Primary DI Number: 03664188000558
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 260432380 *Terms of Use

Device Description: WAM700+ is a multifunctional eye diagnostic device.

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?
65176	Multiple ocular dimension meter	An electrically-powered, ophthalmic device intended to measure multiple dimensional parameters of the eye (e.g., refractive error, corneal anterior surface curvature/thickness, distance between pupils) during an ophthalmic examination, typically to determine a patient's prescription for glasses or evaluate the need for surgery; it not dedicated to measurement of a single dimensional parameter (i.e., it is not a refractometry-, keratometry-, pachymetry-, pupillometry-, or topography-only device). It may be a hand-held or tabletop device, and may be designed for connection to an off-the-shelf computer for device control and/or results analysis/display.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HKX	Tonometer, Ac-Powered
HKO	Refractometer, Ophthalmic
MXK	Device,Analysis,Anterior Segment

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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: 98ff4832-00d0-4461-b1c4-0ca3eede6e3b
Public Version Date: January 15, 2025
Public Version Number: 2
DI Record Publish Date: January 02, 2025

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: No
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

[?]

No Customer Contact currently defined

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