EUROLIGHT C10/E10 SET ophthalmoscope and otoscope

FDA UDI

Class I (US FDA UDI)

by Kirchner & Wilhelm GmbH + Co KG

Identity

Trade Name: EUROLIGHT C10/E10 SET ophthalmoscope and otoscope FDA UDI
Generic Name: Otoscope, direct FDA UDI
Model / Reference: 02.11002.001 FDA UDI

Identifiers

Catalog Number: 02.11002.001 FDA UDI
Primary DI / UDI-DI: 04030155001559 FDA UDI
FDA Product Code: ERA FDA UDI
HLJ FDA UDI
GMDN Term: Otoscope, direct FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4770 FDA UDI
886.1570 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Otoscope, direct Direct ophthalmoscope

EUROLIGHT C10/E10 SET ophthalmoscope and otoscope by Kirchner & Wilhelm GmbH + Co KG — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Kirchner & Wilhelm GmbH + Co KG

Sources (1)

FDA UDI bc3ecdae-846b-45b7-aea2-9685b3a5d038 33 fields · synced Jun 9, 2026