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

156 14+943 61 — Class I MDR by VacuTec Meßtechnik GmbH

MD Atlas
VacuTec Meßtechnik GmbH

EUDAMED last updated this device on Jan 19, 2026

156 14+943 61

++B851VACUDAPBLUETOOTHXH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VacuTec Meßtechnik GmbH
UDI-DI code: +B85115614943610K
Reference / catalog number: 156 14+943 61

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: VacuTec Meßtechnik GmbH
SRN: DE-MF-000006432
Manufacturer status: Active

Critical warnings

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

CW010
Consult instruction for use

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: not provided
UDI-DI code: +B85115614943610K
Basic UDI-DI: ++B851VACUDAPBLUETOOTHXH
Reference / catalog number: 156 14+943 61
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: —
Additional information URL: https://www.vacutec-gmbh.de/en/products/medical/vacudap.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039099VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS – 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

158 00 13++B851VACUDAPOEMUXOn the market 158 00 15++B851VACUDAPOEMUXOn the market 158 00 12++B851VACUDAPOEMUXOn the market 156 00 18++B851VACUDAPOEMUXOn the market 156 00 15++B851VACUDAPOEMUXOn 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.