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

Mech. overflow protection BORA w… — Class I MDR

MD Atlas
ATMOS MedizinTechnik GmbH & Co. KG

EUDAMED last updated this device on Sep 8, 2025

Mech. overflow protection BORA w equipment mount

42503651ACCSYHM5752239279

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ATMOS MedizinTechnik GmbH & Co. KG
UDI-DI code: 04250365183405
Reference / catalog number: HM57522392

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: ATMOS MedizinTechnik GmbH & Co. KG
SRN: DE-MF-000005570
Manufacturer status: Active

Related devices

1-channel endoscope management, ATMOS VideoScope (PED)42503651ACCSYAT53113000YJOn the market ACCUVAC LiteB-04250365193077On the market ACCUVAC Lite with disposable canister systemB-04250365193084On the market ACCUVAC Lite with disposable canister system and accessories bagB-04250365193107On the market ACCUVAC Lite with disposable canister system and power supply unit/ charger for 100 V - 240 VB-04250365193091On 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Medical contra-indications: Home care sector, Operated directly by the patient, Smoke evacuation Other contra-indications: Outside the medical sector. Aspiration of flammable or explosive liquids

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: Mech. overflow protection BORA w equipment mount
UDI-DI code: 04250365183405
Basic UDI-DI: 42503651ACCSYHM5752239279
Reference / catalog number: HM57522392
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)

A0680DRAINAGE AND FLUID COLLECTION DEVICES - 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