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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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TWEEZER / PINZETTA TWEEZER — 33 UDI-DI variants, MDR (AKTIVE SRL)

MD Atlas
AKTIVE SRL

Data from EUDAMED, last updated May 30, 2026

TWEEZER / PINZETTA TWEEZER

8052276FT0002ID1CF

33 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: AKTIVE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8052276FT0002ID1CF
Device name: TWEEZER / PINZETTA TWEEZER
Device model: TWEEZER / PINZETTA TWEEZER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: AKTIVE SRL
SRN: IT-MF-000007813
Country: Italy
Email: quality@aktive-corp.com
Phone: 06.88640509

Variants by status

UDI-DI variants

33 UDI-DI variants

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Applied filters

basicUdiUlid01GK9J8X5SP9YX53BSYDJA7HEB

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

TWEEZER GRIP ASYMMETRICAL 25G08052276028211
TWEEZER JAWS 20G08052276028112
TWEEZER JAWS 23G08052276028266
TWEEZER JAWS 23G (37 mm)08052276028273
TWEEZER JAWS 25G08052276028297
TWEEZER JAWS 25G (37 mm)08052276028303
TWEEZER JAWS 27G08052276028426
TWEEZER JAWS 27G (37mm)08052276028433

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