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Amico Diagnostic Rollstand

FDA UDI

Class II (US FDA UDI)

by Amico Diagnostic Incorporated

Identity

Trade Name
Amico Diagnostic Rollstand FDA UDI
Generic Name
Direct ophthalmoscope FDA UDI
Device Name
Diagnostic Station on Mobile Stand, Ophthal Hal & Oto LED Diagnostic Station Wall Mount, Ophthal Halogen & Oto LED (DI 00697077001308) FDA UDI
Model / Reference
DS-UR1-CHFL-XXX FDA UDI
Description
Diagnostic Station on Mobile Stand, Ophthal Hal & Oto LED Diagnostic Station Wall Mount, Ophthal Halogen & Oto LED (DI 00697077001308) FDA UDI

Identifiers

Primary DI / UDI-DI
00697077002619 FDA UDI
FDA Product Code
HLI FDA UDI
ERA FDA UDI
GMDN Term
Direct ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 FDA UDI
874.4770 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: Direct ophthalmoscope

Amico Diagnostic Rollstand by Amico Diagnostic Incorporated — 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

Sources (1)

  • FDA UDI 45c6206c-a298-4b67-81b2-66c283885912 34 fields · synced May 31, 2026