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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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DUOLITH SD1 T-TOP — 2 UDI-DI variants, MDR (STORZ MEDICAL AG)

MD Atlas
STORZ MEDICAL AG

Data from EUDAMED, last updated May 23, 2026

DUOLITH SD1 T-TOP

76300391ESWT006-TG

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: STORZ MEDICAL AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76300391ESWT006-TG
Device name: DUOLITH SD1 T-TOP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: STORZ MEDICAL AG
SRN: CH-MF-000014374
Country: Switzerland
Email: info@storzmedical.com
Phone: +41 71 677 45 45

Authorised representative

Name: STORZ MEDICAL Deutschland GmbH
SRN: DE-AR-000009017
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KNPG6JMV5N9957T8CX5SS0AX

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

27100.010007630039101695
21362.100007630039101626