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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

ES050-001 — Class I MDD by Surgical Instruments…

MD Atlas
Surgical Instruments Belgium

EUDAMED last updated this device on Apr 4, 2026

ES050-001

B-05407011991627

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Surgical Instruments Belgium
UDI-DI code: 05407011991627
Reference / catalog number: ES050-001

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Manufacturer information

Organization name: Surgical Instruments Belgium
SRN: BE-MF-000029624
Manufacturer status: Active

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13-2-0103-0023B-05407010680997On the market ES028-720B-05407011991337On the market ES025-114B-05407011991078On the market ES024-018B-05407011991023On the market ES021-114B-05407011990927On the market

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05407011991627
Basic UDI-DI: B-05407011991627
Reference / catalog number: ES050-001
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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)

L0205NEEDLE HOLDERS, 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.