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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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QFusion — 1 UDI-DI variant, MDD (Techlamed S.r.l. Unipersonale)

MD Atlas
Techlamed S.r.l. Unipersonale

Data from EUDAMED, last updated May 30, 2026

QFusion

B-08053307980027

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Techlamed S.r.l. Unipersonale

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Device characteristics

Implantable

Legacy certificates

Certificate number: HD60148872
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TUV Rheinland Italia SRL (1936)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08053307980027
Device name: —
Device model: QFusion
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: Techlamed S.r.l. Unipersonale
SRN: IT-MF-000030373
Country: Italy
Email: qualita@techlamed.com
Phone: +39055980070

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01HK9ZXF2ETS35CYH66TWMZ92F

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

QF1208053307980027