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

Stockinette 25x80cm — Class I MDR by BATIST Medical…

MD Atlas
BATIST Medical Productions s.r.o.

EUDAMED last updated this device on May 7, 2026

Stockinette 25x80cm

8596222doc056N2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BATIST Medical Productions s.r.o.
UDI-DI code: 08596222861380
Reference / catalog number: 1220693131

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: BATIST Medical Productions s.r.o.
SRN: CZ-MF-000023495
Manufacturer status: Active

Related devices

Adhesive Aperture Drape 50x60cm, aperture 6x8cm8596222doc047MZOn the market Adhesive Aperture Drape 50x60cm, with aperture 10cm8596222doc047MZOn the market Adhesive Aperture Drape 75x90cm, aperture 6x8cm8596222doc047MZOn the market Adhesive Aperture Drape 80x90cm, with aperture 12cm8596222doc047MZOn the market Adhesive Aperture Drape 90x150cm, aperture 6x18cm8596222doc052MSOn the market

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: Stockinette 25x80cm
UDI-DI code: 08596222861380
Basic UDI-DI: 8596222doc056N2
Reference / catalog number: 1220693131
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: 80 MU10
25 MU10

EMDN nomenclature code(s)

T020199SURGICAL DRAPES - 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

Certificates

Certificate health across this manufacturer's portfolio.

24 0234 QR/NBSupplemented
Quality management systemNotified body: 1023Expiry: Jun 25, 2029