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ri-derma dermatoscope head LED 3.5 V,

FDA UDI

Class I (US FDA UDI)

by Rudolf Riester GmbH & Co. KG

Identity

Trade Name
ri-derma dermatoscope head LED 3.5 V, FDA UDI
Generic Name
Dermatoscope, optical FDA UDI
Device Name
The ri-derma dermascope is produced for early identification of changes of skin pigmentation (malignant melanomas). FDA UDI
Model / Reference
10577-301 FDA UDI
Description
The ri-derma dermascope is produced for early identification of changes of skin pigmentation (malignant melanomas). FDA UDI

Identifiers

Catalog Number
10577-301 FDA UDI
Primary DI / UDI-DI
04045396147171 FDA UDI
FDA Product Code
FSP FDA UDI
GMDN Term
Dermatoscope, optical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dermatoscope, optical

ri-derma dermatoscope head LED 3.5 V, by Rudolf Riester GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatoscope, optical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rudolf Riester GmbH & Co. KG

Sources (1)

  • FDA UDI 7c8f0adf-095a-425c-af7f-59f65e32e51b 34 fields · synced Jun 1, 2026