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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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STOMAFLEX PUTTY — 3 UDI-DI variants, MDR (SpofaDental a.s.)

MD Atlas
SpofaDental a.s.

Data from EUDAMED, last updated May 23, 2026

STOMAFLEX PUTTY

859474710000222B

3 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: SpofaDental a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859474710000222B
Device name: STOMAFLEX PUTTY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: SpofaDental a.s.
SRN: CZ-MF-000000945
Country: Czechia
Email: customerserviceemea@kavokerr.com
Phone: +420 493 583 111

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRHR9PXRRW4AT660JNC7RK0W

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

Stomaflex08594747003360
Stomaflex08594747003353
Stomaflex08594747003346