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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

797.200.29 — Class IIa MDR by Mytronic GmbH

MD Atlas
Mytronic GmbH

EUDAMED last updated this device on Jun 29, 2024

797.200.29

++D95118023JD

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mytronic GmbH
UDI-DI code: +D9511802301004
Reference / catalog number: 797.200.29

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Manufacturer information

Organization name: Mytronic GmbH
SRN: DE-MF-000013849
Manufacturer status: Active

Related devices

797.200.27++D95118023JDOn the market Turbinenschlauch++D95118070JNOn the market Luftmotorschlauch++D95118070JNOn the market 407.794.B01.1600.05.21.98.766++D95118023JDOn the market 794.B57.1350.05.27.98++D95118023JDOn the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: +D9511802301004
Basic UDI-DI: ++D95118023JD
Reference / catalog number: 797.200.29
Issuing entity: HIBCC

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: MC 3FP Spritze (gerade) ohne Schlauch
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q01010199DENTAL RESTORATION 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

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.