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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

DS2.3.3.6.LR — Class IIa MDR by PMT Partners Medische…

MD Atlas
PMT Partners Medische Techniek

EUDAMED last updated this device on May 16, 2025

DS2.3.3.6.LR

8720648STERILIZERX3

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PMT Partners Medische Techniek
UDI-DI code: 08719327514900
Reference / catalog number: DS2.3.3.6.LR

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View device family (Basic UDI)

Manufacturer information

Organization name: PMT Partners Medische Techniek
SRN: NL-MF-000011646
Manufacturer status: Active

Related devices

DS2.3.3.6.DD8720648STERILIZERX3On the market DS2.4.4.6.DD8720648STERILIZERX3On the market DS2.6.6.12.DD8720648STERILIZERX3On the market DS2.6.6.12.ED8720648STERILIZERX3On the market DS2.6.6.16.DD8720648STERILIZERX3On the market

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 2 countries total.

Country	On market since	Until
NetherlandsPrimary placement	May 1, 2025	May 1, 2040
France	May 1, 2025	May 1, 2040

Device identification

Trade name: not provided
UDI-DI code: 08719327514900
Basic UDI-DI: 8720648STERILIZERX3
Reference / catalog number: DS2.3.3.6.LR
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: https://www.pmtpartners.nl/downloads/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08719327514900

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12011380CLEANING, DISINFECTION AND STERILISATION INSTRUMENTS - HARDWARE ACCESSORIES

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

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