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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 — 10 UDI-DI variants, MDR

MD Atlas
LASCOD S.P.A. (LABORATORI SCIENTIFICI ODONTOIATRIA)

Data from EUDAMED, last updated May 31, 2026

BITE

8016200DEROSA001UK

10 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: LASCOD S.P.A. (LABORATORI SCIENTIFICI ODONTOIATRIA)

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8016200DEROSA001UK
Device name: BITE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: LASCOD S.P.A. (LABORATORI SCIENTIFICI ODONTOIATRIA)
SRN: IT-MF-000030743
Country: Italy
Email: quality@lascod.it

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH179VR7DVS4RGFB58333V3W

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

90215718016200022307
KRS09518016200021843
KRS09418016200021836
KRS99318016200022109
KRS97318016200022086
OKR99518016200021102
OKR09518016200020983
OKR09418016200021317
90207018016200021966
90210118016200022192