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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

GreenPulse — Class III MDD by PulseLavage AB

MD Atlas
PulseLavage AB

EUDAMED last updated this device on May 2, 2022

GreenPulse

B-07350093650075

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: PulseLavage AB
UDI-DI code: 07350093650075
Reference / catalog number: GP4000

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View device family (Basic UDI)

Manufacturer information

Organization name: PulseLavage AB
SRN: SE-MF-000002363
Manufacturer status: Active

Related devices

GP4000735009365GPSKHOn the market OrthoLavageB-07350093650013On the market RetraLightB-07350093650556On the market RetraLightB-07350093650600On the market MCS-20735009365MCDJAOn the market

Certificates

Certificate health across this manufacturer's portfolio.

M.2023.1014Cancelled
Quality assuranceNotified body: 2696Expiry: Apr 5, 2028
M.2023.MDR.1013Cancelled
Quality management systemNotified body: 2696Expiry: Apr 5, 2027

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 2 countries total.

Country	On market since	Until
SwedenPrimary placement	Jan 1, 2013	Still on market
Denmark	Jan 1, 2013	Still on market

Device identification

Trade name: GreenPulse
UDI-DI code: 07350093650075
Basic UDI-DI: B-07350093650075
Reference / catalog number: GP4000
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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)07350093650075

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EMDN nomenclature code(s)

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

A03010201ARTHROSCOPIC IRRIGATION CONTROLLERS

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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