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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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Fesia Grasp Pro — 9 UDI-DI variants, MDR (Fesia technology)

MD Atlas
Fesia technology

Data from EUDAMED, last updated May 31, 2026

Fesia Grasp Pro

8437019267GRJM

9 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: Fesia technology

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Device characteristics

Active deviceReusable

Identity & classification

Basic UDI-DI: 8437019267GRJM
Device name: Fesia Grasp Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fesia technology
SRN: ES-MF-000004643
Country: Spain
Email: calidad@fesia.net
Phone: +34943569293

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KSMH8BRCQ7JA6FFQMGQW5D1W

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

ELFR-LM08437019267391
ELFR-LS08437019267384
ELFR-RM08437019267414
ELFR-RS08437019267407
STGA.S2LM08437019267223
STGA.S2LS08437019267216
STGA.S2RM08437019267247
STGA.S2RS08437019267230
STGA.G1008437019267193