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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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PANCAFIT — 4 UDI-DI variants, MDR (POSTURAL SERVICE SRL)

MD Atlas
POSTURAL SERVICE SRL

Data from EUDAMED, last updated May 31, 2026

PANCAFIT

805938891PANCAFITDM

4 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: POSTURAL SERVICE SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805938891PANCAFITDM
Device name: PANCAFIT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: POSTURAL SERVICE SRL
SRN: IT-MF-000048927
Country: Italy
Email: carolina.dambra@posturalservice.it
Phone: 3938495292

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJQARNJR3F9KNDDVHTXDHE0P

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

CAST08059388910038
PANCBLU08059388910014
PANCROSSA08059388910007
PANCVERDE08059388910021