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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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Rescue Instrument — 2 UDI-DI variants, MDR (CeramTec Schweiz GmbH)

MD Atlas
CeramTec Schweiz GmbH

Data from EUDAMED, last updated May 23, 2026

Rescue Instrument

764016139R98130K01RI2A

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: CeramTec Schweiz GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764016139R98130K01RI2A
Device name: Rescue Instrument
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: CeramTec Schweiz GmbH
SRN: CH-MF-000024169
Country: Switzerland
Email: prrc@zeramex.com
Phone: +41782269772

Authorised representative

Name: CeramTec Dentalvertriebs GmbH
SRN: DE-AR-000020220
Country: Germany
Phone: +800 9355 6637

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HWN2W1DX4D17AZ2TXT5JRS7E

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

CERALOG® PL Removal Tool 28mm07640161397286
ZERAMEX® XT Rescue Instrument 28mm07640161397279