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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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STERILNÍ BUNIČITÁ VATA / STERILE… — 5 UDI-DI variants, MDR

MD Atlas
BATIST Medical Productions s.r.o.

Data from EUDAMED, last updated May 23, 2026

STERILNÍ BUNIČITÁ VATA / STERILE CELLULOSE WADDING

8596222CEdoc02FP

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: BATIST Medical Productions s.r.o.

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UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KPTNAJBRZF705XWB6JCF2E5W

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Cellulose Wadding Tampon á10pcs, sterile08596222009492
Cellulose Wadding Tampon á20pcs, sterile08596222005906
Cellulose Wadding Tampon á2pcs, sterile08596222008112
Cellulose Wadding Tampon á3pcs, sterile08596222008211
Cellulose Wadding Tampon á50pcs, sterile08596222008495

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8596222CEdoc02FP
Device name: STERILNÍ BUNIČITÁ VATA / STERILE CELLULOSE WADDING
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: BATIST Medical Productions s.r.o.
SRN: CZ-MF-000023495
Country: Czechia
Email: batist@batist.com

Variants by status