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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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KIJIMEA® REGULARIS — 3 UDI-DI variants, MDR (Synformulas GmbH)

MD Atlas
Synformulas GmbH

Data from EUDAMED, last updated May 23, 2026

KIJIMEA® REGULARIS

PP07498KREG88

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Synformulas GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP07498KREG88
Device name: KIJIMEA® REGULARIS
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: Synformulas GmbH
SRN: DE-MF-000016381
Country: Germany
Email: regulatory@synformulas.com
Phone: +49 (0) 89 / 7879790-78

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HMXTGB687RGKNYWMVS7CGH6Y

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

N/A111924686776
N/A111924687342
N/A111388025018