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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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MACLOREN SUPPOSITORIES — 1 UDI-DI variant, MDD (ADL FARMACEUTICI SRL)

MD Atlas
ADL FARMACEUTICI SRL

Data from EUDAMED, last updated May 31, 2026

MACLOREN SUPPOSITORIES

B-08053306780604

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: ADL FARMACEUTICI SRL

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Legacy certificates

Certificate number: MED-004436-00
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: ICIM S.P.A. (0425)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08053306780604
Device name: MACLOREN SUPPOSITORIES
Device model: RECTAL SUPPOSITORIES
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: ADL FARMACEUTICI SRL
SRN: IT-MF-000037063
Country: Italy
Email: benedetta.buono@adlfarmaceutici.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRE250Y9FQBVNP2Y9QZGK1KC

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

ADL-D13808053306780604