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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

990137101 — Class I MDR by MTW - Endoskopie W.…

MD Atlas
MTW - Endoskopie W. Haag KG

EUDAMED last updated this device on May 7, 2026

990137101

4046223G0304010103ASJJXS7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MTW - Endoskopie W. Haag KG
UDI-DI code: 04046223023415
Reference / catalog number: 990137101

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Manufacturer information

Organization name: MTW - Endoskopie W. Haag KG
SRN: DE-MF-000004993
Manufacturer status: Active

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1006044046223G020199XXXXCSXXXXROn the market 9901307114046223G0304010104ASJXXTWOn the market 9901302024046223G0304010103ASXXXVPOn the market 9901302004046223G0304010103ASXXXVPOn the market 991301311104046223G0304010101ASJXXSPOn the market

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: 04046223023415
Basic UDI-DI: 4046223G0304010103ASJJXS7
Reference / catalog number: 990137101
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G0304010103ERCP CANNULAS, SINGLE-LUMEN, TAPERED TIP

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

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.