Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

ACCESSORIES FOR BIOPSY OR EXPLANT — 3 UDI-DI variants, MDR

MD Atlas
BIOPSYBELL SRL

Data from EUDAMED, last updated May 30, 2026

ACCESSORIES FOR BIOPSY OR EXPLANT

8033860BIOEFT011SJ2

3 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: BIOPSYBELL SRL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: IT349638
Type: refdata.certificate-mdr-type.quality-assurance
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: Feb 10, 2026 → Feb 9, 2030

Identity & classification

Basic UDI-DI: 8033860BIOEFT011SJ2
Device name: ACCESSORIES FOR BIOPSY OR EXPLANT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOPSYBELL SRL
SRN: IT-MF-000011601
Country: Italy
Email: support@biopsybell.it
Phone: +39053527850

Variants by status

UDI-DI variants

3 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KFDHXBYGZ13H1Y8V5ATRETSM

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

ASPYNFINITY08033860008338
ASPYNFINITY08033860004637
ASPYNFINITY08033860022570