Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

16670-LL — Class I MDR by MediTop BV

MD Atlas
MediTop BV

EUDAMED last updated this device on Mar 30, 2026

16670-LL

871810489_CAN_NP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MediTop BV
UDI-DI code: 08718104890114
Reference / catalog number: 16670-LL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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 1030220-SA-ENT871810489_VHL_TROn the market 16670-HZS871810489_CAN_NPOn the market 16690-LL871810489_CAN_NPOn the market

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
Contra-indicated for patient population: • Neonates • Patients with clotting problems • Patients suffering from epidermiolysis bullosa indication Contra-indicated for parts of the body/ tissue used in/ on/ for or to interact with: • Close to exposed viscera and blood vessels • Exposed organs • Necrotic wound bed • Untreated osteomyelitis • Neoplastic tissue in the wound area • Malignant wounds Contra-indicated for use frequency/ duration: Whenever treatment is interrupted or when canister is full.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

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: 08718104890114
Basic UDI-DI: 871810489_CAN_NP
Reference / catalog number: 16670-LL
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 and fixed non-sterile tube with luer-lock connector, length 200 cm.
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)08718104890114

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

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

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

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

Become a partner of MD Atlas

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.