Aladdin Tms

FDA UDI

Class II (US FDA UDI)

by Visia Imaging Srl

Identity

Trade Name: ALADDIN TMS FDA UDI
Generic Name: Corneal topography system analyser FDA UDI
Model / Reference: 1240400 FDA UDI

Identifiers

Catalog Number: 1240400 FDA UDI
Primary DI / UDI-DI: 08034028770180 FDA UDI
510(k) Number: K131567 FDA UDI
FDA Product Code: HJO FDA UDI
GMDN Term: Corneal topography system analyser 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Corneal topography system analyser

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Visia Imaging Srl

Sources (1)

FDA UDI 620e2680-9282-4246-8268-e7e7f41590bb 34 fields · synced May 30, 2026