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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

Clipper SC001 and Charging… — Class I MDR by ME Medical AG

MD Atlas
ME Medical AG

EUDAMED last updated this device on May 4, 2026

Clipper SC001 and Charging Station SC005

7649995SC001A2P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ME Medical AG
UDI-DI code: 07649995283109
Reference / catalog number: SC001 KIT

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Manufacturer information

Organization name: ME Medical AG
SRN: CH-MF-000052198
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Jan 2, 2017	Still on market

Device identification

Trade name: Clipper SC001 and Charging Station SC005
UDI-DI code: 07649995283109
Basic UDI-DI: 7649995SC001A2P
Reference / catalog number: SC001 KIT
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0199CUTTING DEVICES, SINGLE-USE - 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

Related devices

Professional Clipper (single)7649995SC0016AOn the market SC0087649995SC008A3COn the market PG0017649995PG00165On the market SC0027649995SC0026COn the market SC0147649995SC0146KOn 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.