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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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SonicFill 2/SonicFill 3 — 16 UDI-DI variants, MDR (KERR ITALIA SRL)

MD Atlas
KERR ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

SonicFill 2/SonicFill 3

805151187100003357

16 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: 805151187100003357
Device name: SonicFill 2/SonicFill 3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 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

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSPGK07XEX2F0N58E9PDN1HQ

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

SonicFill 208055165091693
SonicFill 208055165091723
SonicFill 208051511877669
SonicFill 208055165091686
SonicFill 208051511877720
SonicFill 208055165091730
SonicFill 208051511877751
SonicFill 208055165091709
SonicFill 208055165091662
SonicFill 208055165091716
SonicFill 208051511877690
SonicFill 208055165091679
SonicFill 308051511877782
SonicFill 308051511877874
SonicFill 308051511877843
SonicFill 308051511877812