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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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Organization name
UDI-DI code
Reference / catalog number

medilogFD — Class IIa MDR by SCHILLER AG

MD Atlas
SCHILLER AG

EUDAMED last updated this device on Jun 11, 2025

medilogFD

761336500000002254

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHILLER AG
UDI-DI code: 07613365004007
Reference / catalog number: 3.900491

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Manufacturer information

Organization name: SCHILLER AG
SRN: CH-MF-000012722
Manufacturer status: Active

Related devices

PB-3000 Var. 476133650000000014UOn the market PB-3000 Var. 7, sub-variant: C (main device 3.921008)76133650000000014UOn the market ARGUS LifePoint761336500000001659On the market ARGUS LifePoint 2761336500000001659On the market ARGUS PB-1000B-07613365000092On the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW023
medilogFD recorder is not to be used in the vicinity of an MR scanner
CW015
medilogFD recorder is BF Classified and is not protected against the effects of defibrillation and/or shocks

Market distribution

Primary placement in Poland; available across 2 countries total.

Country	On market since	Until
PolandPrimary placement		Still on market
France		Still on market

Device identification

Trade name: medilogFD
UDI-DI code: 07613365004007
Basic UDI-DI: 761336500000002254
Reference / catalog number: 3.900491
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12050403ECG HOLTER RECORDERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

G10 041505 0132Issued
Quality management systemNotified body: 0123Expiry: Nov 11, 2026