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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

1030220-ENT — Class I MDR by MediTop BV

MD Atlas
MediTop BV

EUDAMED last updated this device on May 12, 2026

1030220-ENT

871810489_VHL_TR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MediTop BV
UDI-DI code: 08718104890756
Reference / catalog number: 1030220-ENT

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View device family (Basic UDI)

Manufacturer information

Organization name: MediTop BV
SRN: NL-MF-000010795
Manufacturer status: —

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	May 27, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08718104890756
Basic UDI-DI: 871810489_VHL_TR
Reference / catalog number: 1030220-ENT
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: Cordless LED examination headlight for focused illumination during ENT examination and treatment, with adjustable headband, light intensity control and integrated charging. Marketed for Entermed as Enterview III.
Additional information URL: https://www.entermed.com/s/headlights/enterview-3.html
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)08718104890756

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z129004LIGHT SOURCES

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.