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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

LC02 — Class I MDR by Dr. Dimitre Leonidov

MD Atlas
Dr. Dimitre Leonidov

EUDAMED last updated this device on Mar 15, 2022

LC02

426027184LCSFB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Dimitre Leonidov
UDI-DI code: 04260271841672
Reference / catalog number: LC02

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Manufacturer information

Organization name: Dr. Dimitre Leonidov
SRN: DE-MF-000021350
Manufacturer status: Inactive

Related devices

LCM2426027184LCSFBOn the market LC5426027184LCSFBOn the market LC2426027184LCSFBOn the market LCM1426027184LCSFBOn the market LC4426027184LCSFBOn 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

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

CW020
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.
CW138
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: 04260271841672
Basic UDI-DI: 426027184LCSFB
Reference / catalog number: LC02
Issuing entity: GS1

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: Schröpfkopf
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER

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