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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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Manulacer — 4 UDI-DI variants, MDR (Lomed Nederland)

MD Atlas
Lomed Nederland

Data from EUDAMED, last updated May 30, 2026

Manulacer

87188733119BN2

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Lomed Nederland

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87188733119BN2
Device name: Manulacer
Device model: PO 3119-B
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lomed Nederland
SRN: NL-MF-000032807
Country: Netherlands
Email: marketing@lomed.com
Phone: 0880900300

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HF92DEGKSWA2VTKKSEGMYGSJ

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

PO 3119-B08718873036607
PO 3119-B L08718873001285
PO 3119-B M08718873001278
PO 3119-B S08718873001261