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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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WBS BLANKET — 4 UDI-DI variants, MDR (Zeta S.r.l. - MF)

MD Atlas
Zeta S.r.l. - MF

Data from EUDAMED, last updated May 31, 2026

WBS BLANKET

803354931WBSL5

4 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: Zeta S.r.l. - MF

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Device characteristics

Active device

Legacy certificates

Certificate number: IT346520
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: Oct 13, 2025 → Oct 12, 2030

Identity & classification

Basic UDI-DI: 803354931WBSL5
Device name: WBS BLANKET
Device model: WBS Hospital Blanket Full Body
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Zeta S.r.l. - MF
SRN: IT-MF-000017619
Country: Italy
Email: r.riccio@zetagroupsrl.com
Phone: +39 0812785863

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KF11PKZ6FX86FGCHPH392C9Z

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

WBS Emergency Blanket08033549310530
WBS000108033549310554
WBS Hospital Blanket Full Body 2 parts08033549310561
WBS Hospital Blanket Full Body 4 Parts08033549310585