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

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Organization name
UDI-DI code
Reference / catalog number

82520.0842 — Class I MDR by Richard Wolf GmbH

MD Atlas
Richard Wolf GmbH

EUDAMED last updated this device on Nov 8, 2025

82520.0842

405520708032019-0018463K9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Richard Wolf GmbH
UDI-DI code: 04055207033760
Reference / catalog number: 82520.0842

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Manufacturer information

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

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: 04055207033760
Basic UDI-DI: 405520708032019-0018463K9
Reference / catalog number: 82520.0842
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: BRONCHOSCOPE-TUBE ID 11MM OD 13.2 mm, TL 351 mm, for use with the optical element 82510.1400 and head systems 825101100 and 825101200, without distal viewing window, graduated, reusable
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 11 MU50

EMDN nomenclature code(s)

L080899BRONCHOSCOPIC SURGERY INSTRUMENTS, REUSABLE - OTHER

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

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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.