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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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Gravity Waves — 2 UDI-DI variants, MDR (bodyfeed)

MD Atlas
bodyfeed

Data from EUDAMED, last updated May 19, 2026

Gravity Waves

3770034365GWC1BWY

2 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: bodyfeed

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770034365GWC1BWY
Device name: Gravity Waves
Device model: Gravity Waves C1b
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: bodyfeed
SRN: FR-MF-000041782
Country: France
Email: contact@bodyfeedconcept.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HZHZ0HKFM2T0560V4PZVHRF7

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

Gravity Waves C1b - PAG03770034365006
Gravity Waves C1b - PAD03770034365013