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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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Wescott — 1 UDI-DI variant, MDD (M.D.L. S.r.l.)

MD Atlas
M.D.L. S.r.l.

Data from EUDAMED, last updated May 30, 2026

Wescott

B-08052440107216

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: M.D.L. S.r.l.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 166-02-03-DM
Type: refdata.legacy.mdd-certificate-type.v
Notified body: ITALCERT SRL (0426)
Validity: Dec 19, 2023

Identity & classification

Basic UDI-DI: B-08052440107216
Device name: Wescott
Device model: PEW2215
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Feb 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: M.D.L. S.r.l.
SRN: IT-MF-000011599
Country: Italy
Email: info@mdlsrl.com
Phone: +39 0342 682130

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KH6KRJCE7EWWS3NHFKZP15S5

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

PEW221508052440107216