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

VAGINAL APPLICATOR 200 — Class I MDR by Lubelskie Zakłady…

MD Atlas
Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna

EUDAMED last updated this device on Jan 13, 2026

VAGINAL APPLICATOR 200

5906188Aplikatory-kI3U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna
UDI-DI code: 05906188005521
Reference / catalog number: QAPL-0006-000

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: Lubelskie Zakłady Farmaceutyczne "POLFA" Spółka Akcyjna
SRN: PL-MF-000015608
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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 Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Device identification

Trade name: VAGINAL APPLICATOR 200
UDI-DI code: 05906188005521
Basic UDI-DI: 5906188Aplikatory-kI3U
Reference / catalog number: QAPL-0006-000
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

U0899GYNAECOLOGICAL DEVICES - 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

Become a partner of MD Atlas

Related devices

Dosage syringe - volume 5 ml5906188Dozowniki-kImPYOn the market QAPL-0001-0005906188Aplikatory-kI3UOn the market QAPL-0005-0005906188Aplikatory-kI3UOn the market Dosage syringe - volume 10 ml5906188Dozowniki-kImPYOn the market Dosage syringe - volume 10 ml5906188Dozowniki-kImPYOn the market

Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0024/0052/2024Issued
Quality assuranceNotified body: 2274Expiry: Sep 5, 2027