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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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Protective Cap (PEEK) — 8 UDI-DI variants, MDR (anthogyr)

MD Atlas
anthogyr

Data from EUDAMED, last updated May 19, 2026

Protective Cap (PEEK)

36633940006QN

8 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: anthogyr

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 36633940006QN
Device name: —
Device model: Protective Cap (PEEK)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KPMXDTS1BCCVRCE2SQ0Z26RF

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

Axiom03663394001748
Axiom03663394001816
Axiom03663394001779
Axiom03663394001762
Axiom03663394001786
Axiom03663394001755
Axiom03663394001793
Axiom03663394001809