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Myah

FDA UDI

Class II (US FDA UDI)

by Visia Imaging Srl

Identity

Trade Name
MYAH FDA UDI
Generic Name
Corneal topography system FDA UDI
Model / Reference
MYAH FDA UDI

Identifiers

Catalog Number
42-0000983US FDA UDI
Primary DI / UDI-DI
08034028770456 FDA UDI
510(k) Number
K211868 FDA UDI
FDA Product Code
MXK FDA UDI
GMDN Term
Corneal topography system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Corneal topography system

Myah by Visia Imaging Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal topography system.

Cleared under the same submission

K211868 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Visia Imaging Srl

Sources (1)

  • FDA UDI b53fa920-8895-48a9-9643-ab9155179cee 34 fields · synced Jun 8, 2026