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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

11193953721900 — Class I MDR by C+V Pharma Depot GmbH

MD Atlas
C+V Pharma Depot GmbH

EUDAMED last updated this device on May 26, 2026

11193953721900

PP05199EKS22

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C+V Pharma Depot GmbH
UDI-DI code: 111939537219
Reference / catalog number: 11193953721900

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Manufacturer information

Organization name: C+V Pharma Depot GmbH
SRN: DE-MF-000022382
Manufacturer status: Active

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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

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

CW011
Nur zur äußerlichen Anwendung
CW007
EUDAMED did not publish a description for this code.
CW058
EUDAMED did not publish a description for this code.
CW999
Nicht bei Defibrillationsverfahren anwenden.
CW129
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 111939537219
Basic UDI-DI: PP05199EKS22
Reference / catalog number: 11193953721900
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://cuv.copiki.de/w/C%2BV_Pharma
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification