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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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Pulp Canal Sealer — 13 UDI-DI variants, MDR (KERR ITALIA SRL)

MD Atlas
KERR ITALIA SRL

Data from EUDAMED, last updated May 30, 2026

Pulp Canal Sealer

80515118720000055K

13 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: KERR ITALIA SRL

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 80515118720000055K
Device name: Pulp Canal Sealer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: KERR ITALIA SRL
SRN: IT-MF-000007768
Country: Italy
Email: contact.kerritalia@envistaco.com

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRXW7S37GBK29DERWP6CVCX0

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

Pulp Canal Sealer08055165082844
Pulp Canal Sealer08055165082868
Pulp Canal Sealer08055165082875
Pulp Canal Sealer08055165082882
Pulp Canal Sealer08055165082837
Pulp Canal Sealer08055165082806
Pulp Canal Sealer08055165082783
Pulp Canal Sealer08055165082851
Pulp Canal Sealer08055165082899
Pulp Canal Sealer08055165082776
Pulp Canal Sealer08055165082790
Pulp Canal Sealer08055165082813
Pulp Canal Sealer08055165082820