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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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Polsbrace 10" — 11 UDI-DI variants, MDR (Lomed Nederland)

MD Atlas
Lomed Nederland

Data from EUDAMED, last updated May 30, 2026

Polsbrace 10"

8718873PO1106YT

11 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: 8718873PO1106YT
Device name: Polsbrace 10"
Device model: PB PO 1106
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 30, 2023

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

11 UDI-DI variants

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Applied filters

basicUdiUlid01HGFRXQ7YT2TH5J9RE3ACDAC6

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

PB PO 1106R L08718873022853
PB PO 1106R M08718873022860
PB PO 1106L L08718873022808
PB PO 1106L M08718873022815
PB PO 1106L S08718873022822
PB PO 1106L XL08718873022839
PB PO 1106L XS08718873022846
PB PO 1106R S08718873022877
PB PO 1106R XL08718873022884
PB PO 1106R XS08718873022891
PB PO 110608718873036959