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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

V3.3.0 — Class IIa MDR by Pacmed B.V.

MD Atlas
Pacmed B.V.

EUDAMED last updated this device on Jan 28, 2025

V3.3.0

872090823PCX8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pacmed B.V.
UDI-DI code: 08720908230065
Reference / catalog number: V3.3.0

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View device family (Basic UDI)

Manufacturer information

Organization name: Pacmed B.V.
SRN: NL-MF-000010920
Manufacturer status: Active

Related devices

V4.0.0872090823PCX8On the market V3.6.0872090823PCX8On the market V3.2.0872090823PCX8On the market Pacmed Critical872090823PCX8On the market V3.7.0872090823PCX8On 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

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

CW010
IFU

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Feb 3, 2025	Feb 2, 2028

Device identification

Trade name: not provided
UDI-DI code: 08720908230065
Basic UDI-DI: 872090823PCX8
Reference / catalog number: V3.3.0
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720908230065

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EMDN nomenclature code(s)

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

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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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