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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

30-50103.33 — Class IIb MDD by GETSCH+HILLER…

MD Atlas
GETSCH+HILLER Medizintechnik GmbH

EUDAMED last updated this device on May 29, 2026

30-50103.33

B-04059426001340

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: GETSCH+HILLER Medizintechnik GmbH
UDI-DI code: 04059426001340
Reference / catalog number: 30-50103.33

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View device family (Basic UDI)

Manufacturer information

Organization name: GETSCH+HILLER Medizintechnik GmbH
SRN: DE-MF-000007007
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2011	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04059426001340
Basic UDI-DI: B-04059426001340
Reference / catalog number: 30-50103.33
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: Fasszange, lang, mit Löffel, gerieft, Ø5mm, 330mm, db, Einsatz
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04059426001340

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L1299LAPAROSCOPIC AND THORACOSCOPIC INSTRUMENTS, REUSABLE - 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

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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.