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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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BPW1290 — 2 UDI-DI variants, MDR (Smeg S.p.A.)

MD Atlas
Smeg S.p.A.

Data from EUDAMED, last updated May 31, 2026

BPW1290

8017709BPW1290P4

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Smeg S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8017709BPW1290P4
Device name: —
Device model: BPW1290
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Smeg S.p.A.
SRN: IT-MF-000019585
Country: Italy
Email: instruments@smeg.it
Phone: +39 0522 8211

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRKEM1H99PBQ85V6B7D4B831

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

BPW1290J-K508017709346881
BPW1290JEK508017709353735