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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

0116 9041 — Class IIb MDR by PAUSCH Medical GmbH

MD Atlas
PAUSCH Medical GmbH

EUDAMED last updated this device on Nov 18, 2024

0116 9041

4260491620116UR

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PAUSCH Medical GmbH
UDI-DI code: 04260491620163
Reference / catalog number: 0116 9041

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Manufacturer information

Organization name: PAUSCH Medical GmbH
SRN: DE-MF-000011315
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 30, 2019	Still on market
Austria	Oct 23, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260491620163
Basic UDI-DI: 4260491620116UR
Reference / catalog number: 0116 9041
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U99DEVICES FOR UROGENITAL SYSTEM - 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

Related devices

011690424260491620116UROn 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.