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
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- Topographic Modeling System — Tomey Corporation · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Cassini Technologies B.V.
Sources (2)
- FDA UDI a311ee15-1342-4ae5-a917-ead1ad3146d2 34 fields · synced Jun 17, 2026
- EUDAMED 1 fields · synced Jun 1, 2026