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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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GRAPA H.ROS — 6 UDI-DI variants, MDR (SURGIVAL CO., S.A.U.)

MD Atlas
SURGIVAL CO., S.A.U.

Data from EUDAMED, last updated May 23, 2026

GRAPA H.ROS

84352258IMP30600044E

6 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: SURGIVAL CO., S.A.U.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 84352258IMP30600044E
Device name: GRAPA H.ROS
Device model: GRAPA H.ROS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: SURGIVAL CO., S.A.U.
SRN: ES-MF-000028629
Country: Spain
Email: surgival@surgival.com
Phone: +34 961318050

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KPTC2P9E82NSQFNA4XZ7NPSJ

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

H.ROS STAPLE08435225849240
H.ROS STAPLE08435225818772
H.ROS STAPLE08435225818819
H.ROS STAPLE08435225818802
H.ROS STAPLE08435225818789
H.ROS STAPLE08435225818796