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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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Bite Fork — 9 UDI-DI variants, MDR (Itaka Way Med Srl)

MD Atlas
Itaka Way Med Srl

Data from EUDAMED, last updated May 31, 2026

Bite Fork

805903737AccessCyclopsP3

9 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: Itaka Way Med Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805903737AccessCyclopsP3
Device name: Bite Fork
Device model: CYCL.F1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Itaka Way Med Srl
SRN: IT-MF-000030937
Country: Italy
Email: luca.pighin@itakawaymed.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JNKDT1X1X51GSZMSA70F6KT5

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

CYCL.PNT08059037370152
CYCL.F108059037370015
CYCL.F1S08059037370145
CYCL.SUP08059037370060
CYCL.FAL08059037370039
CYCL.FLO08059037370046
CYCL.TR408059037370084
CYCL.T408059037370107
CYCL.OTH08059037370053