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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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Empty guided surgery kit — 5 UDI-DI variants, MDR (anthogyr)

MD Atlas
anthogyr

Data from EUDAMED, last updated May 23, 2026

Empty guided surgery kit

36633940071QZ

5 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: anthogyr

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 36633940071QZ
Device name: —
Device model: Empty guided surgery kit
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: anthogyr
SRN: FR-MF-000000602
Country: France
Email: ra@anthogyr.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KS21BWFE4B7PTPPWSNNKMESY

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

INTEGRAL03663394484381
INTEGRAL03663394484398
INTEGRAL03663394484374
INTEGRAL03663394484367
INMODIGMV03663394481618