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

Ventilution — Class IIa MDR by Gründler GmbH

MD Atlas
Gründler GmbH

EUDAMED last updated this device on Apr 25, 2023

Ventilution

426237137000952BS

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Gründler GmbH
UDI-DI code: 04262371370014
Reference / catalog number: 000070

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: Gründler GmbH
SRN: DE-MF-000025923
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW032
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	Apr 25, 2023	Still on market

Device identification

Trade name: Ventilution
UDI-DI code: 04262371370014
Basic UDI-DI: 426237137000952BS
Reference / catalog number: 000070
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.ggmed.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R9099RESPIRATORY AND ANAESTHESIA DEVICES - 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

Ventilution426237137000951BQOn the market

Certificates

Certificate health across this manufacturer's portfolio.

FI23/00000013refdata.certificate-status.reissued
Quality management systemNotified body: 0598Expiry: Mar 30, 2029
FI23/00000013Issued
Quality management systemNotified body: 0598Expiry: Mar 30, 2026