Pricing Sign in

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.

Filme Gyno-V — 1 UDI-DI variant, MDD (Panin Srl)

MD Atlas
Panin Srl

Data from EUDAMED, last updated May 30, 2026

Filme Gyno-V

B-08033837330158

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Panin Srl

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?

Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: MED31549
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: May 25, 2024

Identity & classification

Basic UDI-DI: B-08033837330158
Device name: Filme Gyno-V
Device model: Filme Gyno-V 6 ovuli_ Filme Gyno-V 2 ovuli
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Nov 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Panin Srl
SRN: IT-MF-000020738
Country: Italy
Email: info@panin.it
Phone: +390425471323

Variants by status

UDI-DI variants

1 UDI-DI variant

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01GHTVHHQFF48ZZYS9ZFVE6J1A

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Filme Gyno-V08033837330158