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Organization name
UDI-DI code
Reference / catalog number

CYSTOSCOPE — Class IIa MDR by Henke-Sass, Wolf GmbH

MD Atlas
Henke-Sass, Wolf GmbH

EUDAMED last updated this device on Feb 25, 2026

CYSTOSCOPE

403587312010106A2

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Henke-Sass, Wolf GmbH
UDI-DI code: 04035873065609
Reference / catalog number: 8300010432

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Manufacturer information

Organization name: Henke-Sass, Wolf GmbH
SRN: DE-MF-000005531
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 1960	Still on market
Austria	Jan 1, 1960	Still on market

Device identification

Trade name: CYSTOSCOPE
UDI-DI code: 04035873065609
Basic UDI-DI: 403587312010106A2
Reference / catalog number: 8300010432
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: "CYST 4/0/300 AK HM ""neu"" HSW modif."
Additional information URL: https://www.henkesasswolf.de/
Clinical sizes: 0°
4,0 mm

EMDN nomenclature code(s)

Z12020701CYSTOSCOPES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

ARTHROSCOPE4035873120101019QOn the market ARTHROSCOPE4035873120101019QOn the market ARTHROSCOPE4035873120101019QOn the market ARTHROSCOPE4035873120101019QOn the market ARTHROSCOPE4035873120101019QOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.