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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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Pelvic blades (St. Mark’s) — 8 UDI-DI variants, MDR

MD Atlas
Ansabere Surgical S.L

Data from EUDAMED, last updated May 23, 2026

Pelvic blades (St. Mark’s)

843657894AN0040CZ

8 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: Ansabere Surgical S.L

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 843657894AN0040CZ
Device name: Pelvic blades (St. Mark’s)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ansabere Surgical S.L
SRN: ES-MF-000006144
Country: Spain
Email: jminsa@ansaberesurgical.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQCQN7SGPVNDS8D99BQNHK74

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

VP35008436578940523
VP35208436578940530
VP37008436578940547
VP37208436578940554
VP350-M08436578944477
VP352-M08436578944484
VP370-M08436578944491
VP372-M08436578944507