← Back to catalogue

Adapters for light cables

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 809509Model 10000201050

by Richard Wolf GmbH

Identity

Trade Name
FUSION DESIGN FDA UDI
Generic Name
Light source adaptor FDA UDI
Device Name
Adapters for light cables EUDAMED
ADAPTER ENDOSCOPE SIDE for connecting a WOLF light cable to WOLF telescopes, quick connect with ring connector, short version, reusable FDA UDI
Model / Reference
10000201050 EUDAMED
809509 EUDAMEDFDA UDI
Description
ADAPTER ENDOSCOPE SIDE for connecting a WOLF light cable to WOLF telescopes, quick connect with ring connector, short version, reusable FDA UDI

Identifiers

Catalog Number
809509 FDA UDI
Primary DI / UDI-DI
04055207038758 EUDAMEDFDA UDI
Basic UDI-DI
405520727052019-0017599Q9 EUDAMED
FDA Product Code
FEM FDA UDI
EMDN Code
Z12020499 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES – OTHER EUDAMED
GMDN Term
Light source adaptor FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
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

Adapters for light cables 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Richard Wolf GmbH
EUDAMED SRN
DE-MF-000007048

Sources (2)

  • EUDAMED 68c3ff99-e1cf-48fa-867c-c389b7429c6e 61 fields · synced Aug 1, 2026
  • FDA UDI 52ae6c3b-9928-408a-9e8d-0443416f713a 35 fields · synced May 30, 2026