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41.0160a

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 41.0160aModel Cystoscopes

by Schölly Fiberoptic Gmbh

Identity

Trade Name
NA FDA UDI
Generic Name
Rigid optical cystoscope FDA UDI
Device Name
Cystoscope 2.9 x 302 mm, 0° FDA UDI
Model / Reference
Cystoscopes EUDAMED
41.0160a EUDAMEDFDA UDI
Description
Cystoscope 2.9 x 302 mm, 0° FDA UDI

Identifiers

Primary DI / UDI-DI
04250480102855 EUDAMEDFDA UDI
04250480103333 EUDAMED
Basic UDI-DI
42504801CYSTOSCOPES7F EUDAMED
Direct Marketing DI
04250480102855 EUDAMED
04250480103333 EUDAMED
FDA Product Code
HIH FDA UDI
FAJ FDA UDI
EMDN Code
Z12020701 CYSTOSCOPES EUDAMED
GMDN Term
Rigid optical cystoscope FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
884.1690 FDA UDI
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

Yes

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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

41.0160a by SCHÖLLY FIBEROPTIC GmbH — Class IIa — 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

EUDAMED SRN
DE-MF-000005618

Sources (3)

  • EUDAMED f98a1dfb-18ae-4bb1-8403-a20c06b917f3 61 fields · synced Aug 3, 2026
  • FDA UDI 506c3531-3659-4604-995c-de9647e7d49c 36 fields · synced May 29, 2026
  • EUDAMED 8854c796-82e3-4245-9296-8484dc8aab54 61 fields · synced Jun 10, 2026