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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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99MB — 2 UDI-DI variants, MDR (99 Technologies SA)

MD Atlas
99 Technologies SA

Data from EUDAMED, last updated May 23, 2026

99MB

76401702699MB00SF

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: 99 Technologies SA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76401702699MB00SF
Device name: 99MB
Device model: 99MB0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: 99 Technologies SA
SRN: CH-MF-000033869
Country: Switzerland
Email: info@99technologies.ch
Phone: +41 91 970 29 29

Authorised representative

Name: Chemsafe s.r.l
SRN: IT-AR-000029957
Country: Italy

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQSAST4R0HKSKMGYX8GMBQJV

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

99MB107640170260205
99MB007640170260083