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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

U-Gel 1000 g Henry Schein HLZ DE — Class I MDR

MD Atlas
C+V Pharma Depot GmbH

EUDAMED last updated this device on May 7, 2026

U-Gel 1000 g Henry Schein HLZ DE

PP05199U.GEL08

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C+V Pharma Depot GmbH
UDI-DI code: 111825236354
Reference / catalog number: A00000848

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View device family (Basic UDI)

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

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

CW007
EUDAMED did not publish a description for this code.
CW129
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Spain		Still on market

Device identification

Trade name: U-Gel 1000 g Henry Schein HLZ DE
UDI-DI code: 111825236354
Basic UDI-DI: PP05199U.GEL08
Reference / catalog number: A00000848
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.

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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