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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

SLH DC — Class IIb MDD by SLH Microtech GmbH

MD Atlas
SLH Microtech GmbH

EUDAMED last updated this device on Oct 13, 2022

SLH DC

B-04260662230153

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: SLH Microtech GmbH
UDI-DI code: 04260662230153
Reference / catalog number: DC 4810

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Manufacturer information

Organization name: SLH Microtech GmbH
SRN: DE-MF-000020864
Manufacturer status: Active

Related devices

SLH DCB-04260662230177On the market SLH DCB-04260662230085On the market SLH DCB-04260662230139On the market SLH DCB-04260662230023On the market SLH DCB-04260662230146On 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.

CW011
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Oct 30, 2020	May 26, 2024
Türkiye	Oct 30, 2020	May 26, 2024

Device identification

Trade name: SLH DC
UDI-DI code: 04260662230153
Basic UDI-DI: B-04260662230153
Reference / catalog number: DC 4810
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Ø: 4.8mm L: 10 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P01020101DENTAL IMPLANTS

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
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Software identification