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pen-scope ophthalmoscope XL 2, 5 V,

FDA UDI

Class II (US FDA UDI)

by Rudolf Riester GmbH & Co. KG

Identity

Trade Name
pen-scope ophthalmoscope XL 2,5 V, FDA UDI
Generic Name
Direct ophthalmoscope FDA UDI
Device Name
The Riester ophthalmoscope has been designed for the examination of the eye and its background. FDA UDI
Model / Reference
2070 FDA UDI
Description
The Riester ophthalmoscope has been designed for the examination of the eye and its background. FDA UDI

Identifiers

Catalog Number
2070 FDA UDI
Primary DI / UDI-DI
04045396002876 FDA UDI
510(k) Number
K932503 FDA UDI
FDA Product Code
HLJ FDA UDI
GMDN Term
Direct ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Direct ophthalmoscope

pen-scope ophthalmoscope XL 2, 5 V, by Rudolf Riester GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Direct ophthalmoscope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d180afc2-20c1-4c61-ac80-9488e5587cbc 35 fields · synced May 30, 2026