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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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Suction unit — 1 UDI-DI variant, MDD (Rossmax Swiss GmbH)

MD Atlas
Rossmax Swiss GmbH

Data from EUDAMED, last updated May 30, 2026

Suction unit

B-764020721V3S2

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: Rossmax Swiss GmbH

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Device characteristics

Active device

Legacy certificates

Certificate number: TW19/20056
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS Belgium NV (1639)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-764020721V3S2
Device name: Suction unit
Device model: V3
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Rossmax Swiss GmbH
SRN: CH-MF-000011245
Country: Switzerland
Email: info@rossmax.com

Authorised representative

Name: CMC Medical Devices & Drugs SL
SRN: ES-AR-000000293
Country: Spain
Phone: +34951214054

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KSHQM8H9ZY6E04Q8ZW71ZJVN

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

Suction unitD-764020721V3S2