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D-Eye

FDA UDI

Class II (US FDA UDI)

by D-Eye Srl

Identity

Trade Name
D-EYE FDA UDI
Generic Name
Direct ophthalmoscope FDA UDI
Device Name
D-EYE for iPhone 6/6S FDA UDI
Model / Reference
DEI0200W1S1400 FDA UDI
Description
D-EYE for iPhone 6/6S FDA UDI

Identifiers

Primary DI / UDI-DI
08053369320014 FDA UDI
FDA Product Code
PJZ FDA UDI
GMDN Term
Direct ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Direct ophthalmoscope

D-Eye by D-Eye Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Direct ophthalmoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
D-Eye Srl

Sources (1)

  • FDA UDI d3003616-2315-45cf-888f-3d02fd1d40b4 33 fields · synced May 30, 2026