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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

ZS0345 — Class IIa MDR by RELIFE S.r.l.

MD Atlas
RELIFE S.r.l.

EUDAMED last updated this device on May 6, 2026

ZS0345

805534824RelizemaCreamJ9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RELIFE S.r.l.
UDI-DI code: 08055348240030
Reference / catalog number: ZS0345

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View device family (Basic UDI)

Manufacturer information

Organization name: RELIFE S.r.l.
SRN: IT-MF-000007611
Manufacturer status: Active

Related devices

ZV0362805534824RelizemaCreamJ9On the market ZS0347805534824RelizemaCreamJ9On the market ZS0348805534824RelizemaCreamJ9On the market ZV0361805534824RelizemaCreamJ9On 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

4 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW999
Do not use in case of hypersensitivity to any of the ingredients
CW275
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Ireland; available across 3 countries total.

Country	On market since	Until
IrelandPrimary placement		Still on market
EL		Still on market
Malta		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08055348240030
Basic UDI-DI: 805534824RelizemaCreamJ9
Reference / catalog number: ZS0345
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: 15
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

EMDN nomenclature code(s)

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

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

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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