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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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GHENESYL silicone-A putty soft NORMAL… — 79 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

GHENESYL silicone-A putty soft NORMAL SET (2x300ml)

8016200DEIMSA001NY

79 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

Clinical investigations

Registered: No

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 8016200DEIMSA001NY
Device name: GHENESYL silicone-A putty soft NORMAL SET (2x300ml)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 5, 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

79 UDI-DI variants

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Applied filters

basicUdiUlid01KGQ7ZKWTGZSRK35SKNX70HTC

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

90210918016200022239
90210818016200022222
90210718016200022215
90214818016200022277

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