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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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PerioCream Periodontal Paste — 1 UDI-DI variant, MDR (bonyf AG)

MD Atlas
bonyf AG

Data from EUDAMED, last updated May 31, 2026

PerioCream Periodontal Paste

7611645PC1800JG

1 UDI-DI variant

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

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

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Device characteristics

No device characteristics flagged

Clinical investigations

Investigation number: CTRI/2014/08/004912
Registered: No
Countries: India

Identity & classification

Basic UDI-DI: 7611645PC1800JG
Device name: PerioCream Periodontal Paste
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: bonyf AG
SRN: LI-MF-000000739
Country: Liechtenstein
Email: administration@bonyf.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQVN0ZJ4ZYC3VGXFE1GV6J3S

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

PerioCream Periodontal Paste07611645329505