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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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Vial Adapter Ø20 Stérilisé SF Sous… — 8 UDI-DI variants, MDR

MD Atlas
UNION PLASTIC

Data from EUDAMED, last updated May 19, 2026

Vial Adapter Ø20 Stérilisé SF Sous blister sans filtre 3X300

3701225715MVADV7

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: UNION PLASTIC

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3701225715MVADV7
Device name: Vial Adapter Ø20 Stérilisé SF Sous blister sans filtre 3X300
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: UNION PLASTIC
SRN: FR-MF-000008940
Country: France
Email: union-plastic@omerin.com
Phone: +33 (0)4 71 61 13 09

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KCGMTQJ8TGK9VY0DP9J3W2FG

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

MEDIC'UP03701225770415
MEDIC'UP03701225770033
MEDIC'UP03701225770224
MEDIC'UP03701225770330
MEDIC'UP03701225770422
MEDIC'UP03701225770361
MEDIC'UP03701225770194
MEDIC'UP03701225770347