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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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RMF UPGRADEKIT TENEO M2 SW1.28 — 1 UDI-DI variant, MDD

MD Atlas
Technolas Perfect Vision GmbH

Data from EUDAMED, last updated May 31, 2026

RMF UPGRADEKIT TENEO M2 SW1.28

B-70009804TPVVL

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: Technolas Perfect Vision GmbH

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Device characteristics

Active device

Legacy certificates

Certificate number: HD 60140657 0001
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-70009804TPVVL
Device name: RMF UPGRADEKIT TENEO M2 SW1.28
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Technolas Perfect Vision GmbH
SRN: DE-MF-000007094
Country: Germany
Email: info@technolaspv.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSM1M91WFM67A29J1D3EJYSB

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

RMF UPGRADEKIT TENEO M2 SW1.28D-70009804TPVVL