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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 00400 — Class I MDR by Vebasan OÜ

MD Atlas
Vebasan OÜ

EUDAMED last updated this device on Jan 11, 2025

EST 00400

426247188ESTBIOCGELDE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vebasan OÜ
UDI-DI code: 04262471880079
Reference / catalog number: EST 00400

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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	Jan 11, 2025	Dec 31, 2025

Device identification

Trade name: not provided
UDI-DI code: 04262471880079
Basic UDI-DI: 426247188ESTBIOCGELDE
Reference / catalog number: EST 00400
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: Calciumgluconat Gel for removel of hydrofluoric acid from uninjured skin and medical devices
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 00300426247188VebaNeutrAllUPOn the market EST 00100426247188VebaNeutrAllUPOn the market EST 00310426247188VebaNeutrAllUPOn 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.