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Cassini

FDA UDIEUDAMED

Class I (US FDA UDI)

by Cassini Technologies B.V.

Identity

Trade Name
CASSINI FDA UDI
Generic Name
Corneal topography system FDA UDI
Device Name
Cassini is a Corneal Topography System. An assembly of ophthalmic devices used to measure the curvature and concentricity of the anterior corneal surface. FDA UDI
Model / Reference
2.0,3.0 FDA UDI
Description
Cassini is a Corneal Topography System. An assembly of ophthalmic devices used to measure the curvature and concentricity of the anterior corneal surface. FDA UDI

Identifiers

Primary DI / UDI-DI
08719326059600 FDA UDI
FDA Product Code
MMQ FDA UDI
GMDN Term
Corneal topography system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1350 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Corneal topography system

Cassini by Cassini Technologies B.V. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Corneal topography system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI a311ee15-1342-4ae5-a917-ead1ad3146d2 34 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026