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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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Rampa s BV — 2 UDI-DI variants, MDR (GAMA GROUP a.s.)

MD Atlas
GAMA GROUP a.s.

Data from EUDAMED, last updated May 23, 2026

Rampa s BV

85935406TF30RAMPYSBVKB

2 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: GAMA GROUP a.s.

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Device characteristics

Administers medicine

Legacy certificates

Certificate number: 26 0129 QR/NB
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390 (1023)
Validity: Apr 30, 2026 → Apr 29, 2031

Identity & classification

Basic UDI-DI: 85935406TF30RAMPYSBVKB
Device name: Rampa s BV
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: GAMA GROUP a.s.
SRN: CZ-MF-000011894
Country: Czechia
Email: gama.jim@gama.cz

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01K5B454YPHQ27WH5ADSATVZHF

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

Ramp 3-way with NP NO PVC M08593540515216
Ramp 5-way with NP NO PVC M08593540515230