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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

9071 — Class IIa MDD by Messer Polska Sp. z o.o.

MD Atlas
Messer Polska Sp. z o.o.

EUDAMED last updated this device on Apr 9, 2024

9071

B-95902768134288

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Messer Polska Sp. z o.o.
UDI-DI code: 95902768134288
Reference / catalog number: 9071

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View device family (Basic UDI)

Manufacturer information

Organization name: Messer Polska Sp. z o.o.
SRN: PL-MF-000001609
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 95902768134288
Basic UDI-DI: B-95902768134288
Reference / catalog number: 9071
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Azot medyczny skroplony MESSERMEDLINE - CRYOLIN do krioterapii, kriochirurgii i krioprezerwacji jest wyrobem przeznaczonym do profesjonalnego używania podczas zabiegów krioterapii miejscowej, ogólnoustrojowej, zabiegów kriochirurgii i w procesie krioprezerwacji.
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)95902768134288

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EMDN nomenclature code(s)

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

V0902CLINICAL/THERAPEUTIC APPLICATIONS LIQUID NITROGEN

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

9032B-95902768134271On 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.