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

VM-104/2 — Class I MDR by VAKUFORM s.r.o.

MD Atlas
VAKUFORM s.r.o.

EUDAMED last updated this device on May 5, 2026

VM-104/2

859422551VAKUFORMHR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VAKUFORM s.r.o.
UDI-DI code: 08594225510991
Reference / catalog number: VM-104/2

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: VAKUFORM s.r.o.
SRN: CZ-MF-000044602
Manufacturer status: Active

Market distribution

Primary placement in Czechia; available across 3 countries total.

Country	On market since	Until
CzechiaPrimary placement		Still on market
Romania		Still on market
Slovakia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594225510991
Basic UDI-DI: 859422551VAKUFORMHR
Reference / catalog number: VM-104/2
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: Vakuové matrace jsou mnohonásobně použitelné fixační prostředky pro poskytnutí přednemocniční neodkladné péče. Jsou určeny k šetrné stabilizaci a transportní imobilizaci při poranění páteře a při mnohačetných poraněních (např. se zlomeninami v pánevní oblasti).
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050103EMERGENCY AND TRAUMATOLOGY STRETCHERS

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

VS-117859422551VAKUFORMHROn the market VS-105859422551VAKUFORMHROn the market VS-104859422551VAKUFORMHROn the market VS-109859422551VAKUFORMHROn the market VS-108859422551VAKUFORMHROn 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.