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

801 — Class I MDD by BSV Kubiš, s.r.o.

MD Atlas
BSV Kubiš, s.r.o.

EUDAMED last updated this device on Jul 14, 2025

801

B-CZMF000040605801XF

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: BSV Kubiš, s.r.o.
UDI-DI code: D-CZMF000040605801XF
Reference / catalog number: 801

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: BSV Kubiš, s.r.o.
SRN: CZ-MF-000040605
Manufacturer status: Active

Related devices

103B-CZMF000040605103WGOn the market 802B-CZMF000040605802XHOn the market 505B-CZMF000040605505X8On the market 402B-CZMF000040605402WVOn the market 304B-CZMF000040605304WUOn the market

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.

Market distribution

Primary placement in Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-CZMF000040605801XF
Basic UDI-DI: B-CZMF000040605801XF
Reference / catalog number: 801
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: nerez
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 0.7 MU50
55 MU50

EMDN nomenclature code(s)

L0202SUTURE NEEDLES, REUSABLE

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