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.

SPRAY GOLA FAMILY — 6 UDI-DI variants, MDR (Labomar S.p.A.)

MD Atlas
Labomar S.p.A.

Data from EUDAMED, last updated May 31, 2026

SPRAY GOLA FAMILY

805630062FTPR1297

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Labomar S.p.A.

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

Clinical investigations

Registered: No

Legacy certificates

Certificate number: CSQ0026240424
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Nov 25, 2024 → Oct 27, 2029

Identity & classification

Basic UDI-DI: 805630062FTPR1297
Device name: SPRAY GOLA FAMILY
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Labomar S.p.A.
SRN: IT-MF-000007965
Country: Italy
Email: regulatoryMD@labomar.com
Phone: +3904227312

Variants by status

UDI-DI variants

6 UDI-DI variants

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

basicUdiUlid01K0P2ZMYDJHCEWC8A45H9R2TM

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

FTPR1208056300621065
FTPR1208056300621225
FTPR1208056300621805
FTPR1208056300621027
FTPR1208056300621331
SPRAY MAL DE GORGE FR08056300620952