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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

EST 0100 x 4 — Class I MDR by Vebasan OÜ

MD Atlas
Vebasan OÜ

EUDAMED last updated this device on Apr 13, 2026

EST 0100 x 4

4280001912BodyNeutrAll2FU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vebasan OÜ
UDI-DI code: 04262471880246
Reference / catalog number: EST 0100 x 4

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Manufacturer information

Organization name: Vebasan OÜ
SRN: EE-MF-000043782
Manufacturer status: Active

Market distribution

Primary placement in Estonia; available across 1 country total.

Country	On market since	Until
EstoniaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262471880246
Basic UDI-DI: 4280001912BodyNeutrAll2FU
Reference / catalog number: EST 0100 x 4
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: EST 0100 * 2
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

EST 003004280001912BodyNeutrAll2FUOn the market EST 003004280001912BodyNeutrAll2FUOn the market EST 00400426247188ESTBIOCGELDEOn the market EST 00300426247188VebaNeutrAllUPOn the market EST 00100426247188VebaNeutrAllUPOn 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.