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

99130101210 — Class I MDR by MTW - Endoskopie W.…

MD Atlas
MTW - Endoskopie W. Haag KG

EUDAMED last updated this device on May 7, 2026

99130101210

4046223G020199XXXXBSXXXXE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MTW - Endoskopie W. Haag KG
UDI-DI code: 04046223040740
Reference / catalog number: 99130101210

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

Related devices

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: 04046223040740
Basic UDI-DI: 4046223G020199XXXXBSXXXXE
Reference / catalog number: 99130101210
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)

G020199GASTROINTESTINAL LAVAGE, TUBES AND SETS - 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

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.