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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

PP01-01 — Class IIa MDR by Medinice S.A.

MD Atlas
Medinice S.A.

EUDAMED last updated this device on Apr 29, 2026

PP01-01

59038873766PP018G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medinice S.A.
UDI-DI code: 05903887376631
Reference / catalog number: PP01-01

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View device family (Basic UDI)

Manufacturer information

Organization name: Medinice S.A.
SRN: PL-MF-000026941
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement	Mar 1, 2027	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05903887376631
Basic UDI-DI: 59038873766PP018G
Reference / catalog number: PP01-01
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: Wyrób medyczny PacePress® służy do kompresji miejsca implantacji CIED* w celu zapobiegania powstawania krwiaków.
Additional information URL: No additional information URL provided by the manufacturer.
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)05903887376631

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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.

Z120607PNEUMATIC COMPRESSION EQUIPMENT

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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Related devices

PP01-11 59038873766PP018GOn the market

Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0032/5013/2025Issued
Quality management systemNotified body: 2274Expiry: Feb 23, 2030