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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 8'' — 11 UDI-DI variants, MDR (Lomed Nederland)

MD Atlas
Lomed Nederland

Data from EUDAMED, last updated May 30, 2026

Polsbrace 8''

8718873PO1101YH

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: 8718873PO1101YH
Device name: Polsbrace 8''
Device model: PB PO 1101
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

basicUdiUlid01HGFRHY8Z0ZFKMMD350DTZYV4

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 110108718873036942
PB PO 1101L L08718873022709
PB PO 1101L M08718873022716
PB PO 1101L S08718873022723
PB PO 1101L XL08718873022730
PB PO 1101L XS08718873022747
PB PO 1101R L08718873022754
PB PO 1101R M08718873022761
PB PO 1101R S08718873022778
PB PO 1101R XL08718873022785
PB PO 1101R XS08718873022792