Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

11195491315600 — 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

11195491315600

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: 111954913156
Reference / catalog number: 11195491315600

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

A00001511PP05199E.GEL58On the market A00001209PP05199E.GEL58On the market A00001149PP05199E.GEL58On the market E-Gel 250 g Henry Schein HSPP05199E.GEL58On the market A00001204PP05199E.GEL58On 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

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.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 111954913156
Basic UDI-DI: PP05199EKS22
Reference / catalog number: 11195491315600
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