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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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VAGINAL GELS — 5 UDI-DI variants, MDR (Crab Sinergy Srl)

MD Atlas
Crab Sinergy Srl

Data from EUDAMED, last updated May 31, 2026

VAGINAL GELS

8033776702287001J3

5 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: Crab Sinergy Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8033776702287001J3
Device name: —
Device model: VAGINAL GELS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Oct 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Crab Sinergy Srl
SRN: IT-MF-000008825
Country: Italy
Email: info@crabsinergy.com
Phone: +39035973286

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K7RMDXD3KZTY111MTMSPANE1

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

VHG005 IT08033776701316
HYALSOLO GEL08033776700944
PLANFERTIL GEL08033776700869
VHG002 MY08033776701361
VHG 00108033776700753