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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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Pro28F — 57 UDI-DI variants, MDR (Puma Srl)

MD Atlas
Puma Srl

Data from EUDAMED, last updated May 31, 2026

Pro28F

805750785P28FZ12149002ZP

57 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: Puma Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805750785P28FZ12149002ZP
Device name: Pro28F
Device model: Pro28F
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Puma Srl
SRN: IT-MF-000047643
Country: Italy
Email: mauro.muselli@pumasrl.it
Phone: +39 347 3862578

Variants by status

UDI-DI variants

57 UDI-DI variants

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Applied filters

basicUdiUlid01JVPZMWB5VKNF27WZHHKG3E9P

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

PRO 28F08057507850432
PRO 28F08057507850487
PRO 28F08057507850494
pro 28 F08057507850449
pro 28 F08057507851385
PRO 28F08057507851224
PRO 28F08057507850401

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