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Light rods for light source connection

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 824202001Model 10000201386

by Richard Wolf GmbH

Identity

Trade Name
NA FDA UDI
Generic Name
Rigid intubation laryngoscope, reusable FDA UDI
Device Name
Light rods for light source connection EUDAMED
LIGHT CARRIER FOR LARYNGOSCOPE external, for operating laryngoscopes 824202000 FDA UDI
Model / Reference
10000201386 EUDAMED
824202001 EUDAMEDFDA UDI
Description
LIGHT CARRIER FOR LARYNGOSCOPE external, for operating laryngoscopes 824202000 FDA UDI

Identifiers

Catalog Number
824202001 FDA UDI
Primary DI / UDI-DI
04055207033326 EUDAMEDFDA UDI
Basic UDI-DI
405520727052019-0018513PC EUDAMED
Direct Marketing DI
04055207033326 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12020480 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Rigid intubation laryngoscope, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Light rods for light source connection by Richard Wolf GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH
EUDAMED SRN
DE-MF-000007048

Sources (2)

  • EUDAMED 7caf18c2-7221-4090-95e4-d1fdd1f72ace 61 fields · synced Jul 16, 2026
  • FDA UDI cb170dcb-48e1-41ba-8c62-df50e0fab45d 36 fields · synced May 30, 2026