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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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BPL33TP — 3 UDI-DI variants, MDR (BIOLOGITECH SRL)

MD Atlas
BIOLOGITECH SRL

Data from EUDAMED, last updated May 31, 2026

BPL33TP

805951396A14JK

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: BIOLOGITECH SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805951396A14JK
Device name: BPL33TP
Device model: Boccole per implantologia
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOLOGITECH SRL
SRN: IT-MF-000024415
Country: Italy
Email: info@biologitech.it
Phone: +39 0 255 30 04 56

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS2E6P4PYQF70KPN347G54R0

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

Bushing d.4.0mm 3Pcs pack08059513962741
Bushing d.5.0mm 3Pcs pack08059513962758
Bushing d.6.0mm 3Pcs pack08059513962765