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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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FLEXOR MEDICAL CARE PIE CAVO — 6 UDI-DI variants, MDR (Flexor S.A.)

MD Atlas
Flexor S.A.

Data from EUDAMED, last updated May 23, 2026

FLEXOR MEDICAL CARE PIE CAVO

84355156FM7270CW

6 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: Flexor S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84355156FM7270CW
Device name: FLEXOR MEDICAL CARE PIE CAVO
Device model: FLEXOR MEDICAL CARE PIE CAVO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Flexor S.A.
SRN: ES-MF-000042891
Country: Spain
Email: quality@flexor.es
Phone: +34 93 718 16 12

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JZ2MP9J06A26CB8Z1ACZWDRG

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

FM7 270 35/3608435515600179
FM7 270 37/3808435515600186
FM7 270 39/4008435515600193
FM7 270 41/4208435515600209
FM7 270 43/4408435515600216
FM7 270 45/4608435515600223