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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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MOVICOL® Ready to Take — 1 UDI-DI variant, MDD (Norgine BV)

MD Atlas
Norgine BV

Data from EUDAMED, last updated May 30, 2026

MOVICOL® Ready to Take

B-05012748606227

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Norgine BV

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: HD 1676230-1
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-05012748606227
Device name: MOVICOL® Ready to Take
Device model: 77710084 (30s)
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Nov 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Norgine BV
SRN: NL-MF-000009565
Country: Netherlands
Email: apatel2@norgine.com
Phone: ++44 740814916

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01H8YC458138H59CJGFNNAMCCS

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

MOVICOL® Ready to Take05012748606227