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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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Acetocaustin 2 ml — 1 UDI-DI variant, MDD (PK Benelux BV)

MD Atlas
PK Benelux BV

Data from EUDAMED, last updated May 30, 2026

Acetocaustin 2 ml

B-073415NS

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: PK Benelux BV

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: Z/19/04409E
Type: refdata.legacy.mdd-certificate-type.v
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Jan 31, 2023

Identity & classification

Basic UDI-DI: B-073415NS
Device name: Acetocaustin 2 ml
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: PK Benelux BV
SRN: NL-MF-000006672
Country: Netherlands
Email: a.steenbergen_peters@pkbenelux.com
Phone: +31413253338

Variants by status

UDI-DI variants

1 UDI-DI variant

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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

Acetocaustin 2 mlD-073415NS