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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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CAMLOG® Re-Set — 4 UDI-DI variants, MDR (ALTATEC GmbH)

MD Atlas
ALTATEC GmbH

Data from EUDAMED, last updated May 23, 2026

CAMLOG® Re-Set

40997970004028000000000LB

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ALTATEC GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40997970004028000000000LB
Device name: CAMLOG® Re-Set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: ALTATEC GmbH
SRN: DE-MF-000006230
Country: Germany
Email: raphael.brausch@altatec.de
Phone: +49-70449445-311

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KN46HSNJMYQYZX709V3C3HAC

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

CAMLOG® Re-Set Removal set04099797013429
CAMLOG® Re-Set Removal set04099797013405
CAMLOG® Re-Set Removal set04099797013436
CAMLOG® Re-Set Removal set04099797013412