Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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

Suction catheter Ch 6 — Class IIa MDD by Hrvatski zavod za…

MD Atlas
Hrvatski zavod za transfuzijsku medicinu

EUDAMED last updated this device on Aug 18, 2022

Suction catheter Ch 6

B-021700125H

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Hrvatski zavod za transfuzijsku medicinu
UDI-DI code: D-021700125H
Reference / catalog number: 02170012

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?

Manufacturer information

Organization name: Hrvatski zavod za transfuzijsku medicinu
SRN: HR-MF-000019208
Manufacturer status: Active

Related devices

Abdominal drain Ch 22B-0234000155On the market Abdominal drain Ch 24B-0234000257On the market Abdominal drain Ch 26B-0234000359On the market Abdominal drain Ch 28B-023400045BOn the market Abdominal drain Ch 30B-023400055DOn the market

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Croatia; available across 1 country total.

Country	On market since	Until
CroatiaPrimary placement		Still on market

Device identification

Trade name: Suction catheter Ch 6
UDI-DI code: D-021700125H
Basic UDI-DI: B-021700125H
Reference / catalog number: 02170012
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: For tracheobronchial suction of the lungs, throat and nose.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2 MU50
520 MU50

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

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.