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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

2001 — Class I MDR by Bernhard Hermle GmbH

MD Atlas
Bernhard Hermle GmbH

EUDAMED last updated this device on Mar 24, 2026

2001

426072582Ir-TrephinKorSF9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bernhard Hermle GmbH
UDI-DI code: 04260725822417
Reference / catalog number: 2001

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Manufacturer information

Organization name: Bernhard Hermle GmbH
SRN: DE-MF-000010226
Manufacturer status: Active

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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.

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: 04260725822417
Basic UDI-DI: 426072582Ir-TrephinKorSF9
Reference / catalog number: 2001
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: LASEK-Trepan mit Fadenkreuz, Ø 8,0mm, 105mm
Additional information URL: https://www.hermle-medizintechnik.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L170401CORNEAL TREPHINES, REUSABLE

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

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