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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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AFB SAFEBAG KV — 2 UDI-DI variants, MDR (Vantive Health GmbH)

MD Atlas
Vantive Health GmbH

Data from EUDAMED, last updated May 31, 2026

AFB SAFEBAG KV

7332414VA0000412V

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Vantive Health GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7332414VA0000412V
Device name: AFB SAFEBAG KV
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Vantive Health GmbH
SRN: CH-MF-000038981
Country: Switzerland
Email: fabrizio.pasqua@vantive.com
Phone: +41 7974 68 216

Authorised representative

Name: Vantive S.r.l.
SRN: IT-AR-000041309
Country: Italy

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KSH44TS5RACHESSQJQ3VPTWW

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

AFB SAFEBAG KV07332414069629
AFB SAFEBAG KV07332414066017