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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Menthol Gel - Cryotherapy — 1 UDI-DI variant, MDD

MD Atlas
LABIALFARMA – LABORATÓRIO DE PRODUTOS FARMACÊUTICOS E NUTRACÊUTICOS, S.A.

Data from EUDAMED, last updated May 31, 2026

Menthol Gel - Cryotherapy

B-05601653008969

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: LABIALFARMA – LABORATÓRIO DE PRODUTOS FARMACÊUTICOS E NUTRACÊUTICOS, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-05601653008969
Device name: Menthol Gel - Cryotherapy
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jun 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: LABIALFARMA – LABORATÓRIO DE PRODUTOS FARMACÊUTICOS E NUTRACÊUTICOS, S.A.
SRN: PT-MF-000003551
Country: Portugal
Email: mdvigilance@labialfarma.com
Phone: +351 231 927 590

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01JYEPXFATK98CTNDQMHSJQV7K

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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

MGC00105601653008969