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Organization name
UDI-DI code
Reference / catalog number

ti1004 — Class IIa MDR by tic Medizintechnik GmbH

MD Atlas
tic Medizintechnik GmbH

EUDAMED last updated this device on Feb 4, 2026

ti1004

426021766-T-PLSH

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: tic Medizintechnik GmbH
UDI-DI code: 04260217666185
Reference / catalog number: ti1004

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Manufacturer information

Organization name: tic Medizintechnik GmbH
SRN: DE-MF-000033923
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
Siehe Kapitel Warn- und Sicherheitshinweise und Kontraindikationen

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Mar 31, 2001	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260217666185
Basic UDI-DI: 426021766-T-PLSH
Reference / catalog number: ti1004
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: syntic - EMG-getriggertes Elektrostimulations-System zur Inkontinenztherapie (Kombination Biofeedback + Elektrostimulation)
Additional information URL: https://ticmed.de/downink/Bedienungsanleitung%20syntic%20022025R14TIC.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0499INCONTINENCE DEVICES - OTHER

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

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.