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

1656 — Class I MDR by NOUVAG AG

MD Atlas
NOUVAG AG

EUDAMED last updated this device on May 20, 2026

1656

++ENOU100032LJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NOUVAG AG
UDI-DI code: +ENOU19569X
Reference / catalog number: 1656

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: NOUVAG AG
SRN: CH-MF-000018882
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 15, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: +ENOU19569X
Basic UDI-DI: ++ENOU100032LJ
Reference / catalog number: 1656
Issuing entity: HIBCC

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: Surgical irrigation nozzle intended as accessory to direct irrigation fluids to the surgical site for rinsing, removal of debris, and cooling during surgical procedures.
Additional information URL: https://www.nouvag.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019080VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - HARDWARE ACCESSORIES
Z12110180INSTRUMENTS FOR DENTAL TREATMENT UNITS - HARDWARE ACCESSORIES
Z12149080VARIOUS ENT INSTRUMENTS - HARDWARE ACCESSORIES

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

19869++ENOU100033LLOn the market 1964++ENOU100032LJOn the market 1932spi++ENOU100032LJOn the market 1966++ENOU100032LJOn the market 1935spi++ENOU100032LJOn 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.