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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-SA-ENT — Class I MDR by MediTop BV

MD Atlas
MediTop BV

EUDAMED last updated this device on May 12, 2026

1030220-SA-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: 08718104890923
Reference / catalog number: 1030220-SA-ENT

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View device family (Basic UDI)

Manufacturer information

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

Related devices

5526653ASY871810489_CAN_NPOn the market 1030220-ENT871810489_VHL_TROn the market 16670-LL871810489_CAN_NPOn the market 16670-HZS871810489_CAN_NPOn the market 16690-LL871810489_CAN_NPOn the market

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: 08718104890923
Basic UDI-DI: 871810489_VHL_TR
Reference / catalog number: 1030220-SA-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 standalone charging holder. 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)08718104890923

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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.