Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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.

Jednorázová rouška Balerina BFE99 — 144 UDI-DI variants, MDR

MD Atlas
Balerina-Czech, s.r.o.

Data from EUDAMED, last updated May 23, 2026

Jednorázová rouška Balerina BFE99

859420537BFE99CA

144 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: Balerina-Czech, s.r.o.

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?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420537BFE99CA
Device name: Jednorázová rouška Balerina BFE99
Device model: BFE99
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Balerina-Czech, s.r.o.
SRN: CZ-MF-000050806
Country: Czechia
Email: info@balerina.cz

Variants by status

UDI-DI variants

144 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KFB8MJD3H19ZEAX9Y3C5ZVQ1

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

859420537711808594205377118
859420537757608594205377576
859420537623408594205376234
859420537628908594205376289
859420537637108594205376371
859420537690608594205376906
859420537608108594205376081
859420537621008594205376210
859420537614208594205376142
859420537728608594205377286
859420537672208594205376722
859420537715608594205377156
859420537645608594205376456
859420537718708594205377187
859420537616608594205376166
859420537697508594205376975
859420537745308594205377453
859420537707108594205377071
859420537643208594205376432
859420537657908594205376579
859420537640108594205376401
859420537627208594205376272
859420537720008594205377200
859420537642508594205376425
859420537671508594205376715

1 2 3 4 5