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Cleaning Brush CS-C9S

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6217001Z866SModel See UDI-DI information for model names

by HOYA Corporation

Identity

Trade Name
Cleaning Brush CS-C9S EUDAMED
PENTAX FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Device Name
PENTAX Medical Cleaning Brush EUDAMED
Cleaning Brush CS-C9S FDA UDI
Model / Reference
See UDI-DI information for model names EUDAMED
6217001Z866S EUDAMED
CS-C9S FDA UDI
Description
Cleaning Brush CS-C9S FDA UDI

Identifiers

Primary DI / UDI-DI
04961333129478 EUDAMEDFDA UDI
Basic UDI-DI
4961333010507YC EUDAMED
FDA Product Code
MNL FDA UDI
EMDN Code
V070101 ENDOSCOPES CLEANING BRUSHES - FOR GENERIC USE EUDAMED
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable 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

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

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: Surgical instrument/endoscope cleaning utensil, single-use

Cleaning Brush CS-C9S by HOYA Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
HOYA Corporation
EUDAMED SRN
JP-MF-000005227
Authorised Representative
PENTAX Europe GmbH DE-AR-000000006

Sources (2)

  • EUDAMED bde648d2-fe3e-4faf-9497-d6ca87c54bf1 61 fields · synced Jun 19, 2026
  • FDA UDI ff3920ab-6590-4270-86fa-b0fee5d6da8e 33 fields · synced May 30, 2026