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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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Scanbody ScanFlagIQ — 9 UDI-DI variants, MDR (NEW ANCORVIS SRL)

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 31, 2026

Scanbody ScanFlagIQ

08053876KSL00JJ

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: NEW ANCORVIS SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08053876KSL00JJ
Device name: Scanbody ScanFlagIQ
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: NEW ANCORVIS SRL
SRN: IT-MF-000008879
Country: Italy
Email: qualita@newancorvis.eu
Phone: +390516463070

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KR3SNR3CYYEEQ61C79VMFG0K

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

KIT-SF101708053876098215
KIT-SF02708053876098178
KIT-SF26008053876098383
KIT-SF93608053876098185
KIT-SF01408053876098222
KIT-SF23708053876099298
KIT-SF23808053876099304
KIT-SF101608053876098192
KIT-SF25508053876098208