Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

8836.19 — Class I MDR by Richard Wolf GmbH

MD Atlas
Richard Wolf GmbH

EUDAMED last updated this device on Nov 8, 2025

8836.19

405520727052019-0018189PR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Richard Wolf GmbH
UDI-DI code: 04055207011225
Reference / catalog number: 8836.19

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Richard Wolf GmbH
SRN: DE-MF-000007048
Manufacturer status: Active

Related devices

8108233405520720052019-0017627DCOn the market 8108253405520720052019-0017627DCOn the market 5525201405520724072019-0017684N6On the market 5525105405520724072019-0017684N6On the market 8108.152405520720052019-0017627DCOn 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04055207011225
Basic UDI-DI: 405520727052019-0018189PR
Reference / catalog number: 8836.19
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: PROCTOSCOPE TUBE Ø 20MM WL 148MM WL 148mm, TL 163mm, cylindrical with lateral window, reusable
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 148 MU50
20 MU50

EMDN nomenclature code(s)

L0406RIGID RECTOSCOPES AND ANOSCOPES, REUSABLE

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