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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

16670-HZS — Class I MDR by MediTop BV

MD Atlas
MediTop BV

EUDAMED last updated this device on May 12, 2026

16670-HZS

871810489_CAN_NP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MediTop BV
UDI-DI code: 08718104890121
Reference / catalog number: 16670-HZS

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Manufacturer information

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

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW008
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW999
Use of the device is contra-indicated for the following patient population: • Neonates • Patients with clotting problems • Patients suffering from epidermiolysis bullosa indication Use of the device is contra-indicated for the following parts of the body/ tissue used in/ on/ for or to interaction with: • Close to exposed viscera and blood vessels • Exposed organs • Necrotic wound bed • Untreated osteomyelitis • Neoplastic tissue in the wound area • Malignant wounds Use of the device is contra-indicated for the following use frequency/ duration: • Whenever treatment is interrupted or when canister is full.

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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: 08718104890121
Basic UDI-DI: 871810489_CAN_NP
Reference / catalog number: 16670-HZS
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: Disposable canister, 900 cc with filter, without tube.
Additional information URL: https://www.meditop.com/producten/negative-pressure-wound-therapy/exsudex.html
Clinical sizes: 900 MU48

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08718104890121

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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.

A0680DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES

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.