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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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Florence 215 — 1 UDI-DI variant, MDD (Maxeta AS)

MD Atlas
Maxeta AS

Data from EUDAMED, last updated May 30, 2026

Florence 215

B-70706820345114

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: Maxeta AS

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Device characteristics

Administers medicine

Legacy certificates

Certificate number: 10000445936-PA-NA-NOR
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DNV Product Assurance AS (2460)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-70706820345114
Device name: Florence 215
Device model: P201-215
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Oct 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Maxeta AS
SRN: NO-MF-000015725
Country: Norway
Email: maxeta@maxeta.no
Phone: +47 35914000

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GG4M0YR31FFDKG8N15HZR6W0

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

P201-21570706820345114