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.

DibuCell ACTIVE AKTYWNY OPATRUNEK… — 1 UDI-DI variant, MDD

MD Atlas
Celther Polska Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

DibuCell ACTIVE AKTYWNY OPATRUNEK PRZYSPIESZAJĄCY GOJENIE RAN

B-05905669556088

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Celther Polska Sp. z o.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

Animal tissues / cells

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 1434-MDD-587/2019
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: Aug 10, 2022

Identity & classification

Basic UDI-DI: B-05905669556088
Device name: DibuCell ACTIVE AKTYWNY OPATRUNEK PRZYSPIESZAJĄCY GOJENIE RAN
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Jul 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: Celther Polska Sp. z o.o.
SRN: PL-MF-000002202
Country: Poland
Email: agnieszka.oszczypko@celther.com
Phone: +48509782538

Variants by status

UDI-DI variants

1 UDI-DI variant

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

basicUdiUlid01G7SC1CRWAYK14J5510S52NSN

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

DibuCell ACTIVE ACTIVE DRESSING MATERIAL ACCELERATING WOUND HEALING05905669556088