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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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Fluido® Pressure Chamber — 1 UDI-DI variant, MDR

MD Atlas
The Surgical Company International B.V.

Data from EUDAMED, last updated May 31, 2026

Fluido® Pressure Chamber

8719867EMDNZ12030380PCK4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: The Surgical Company International B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8719867EMDNZ12030380PCK4
Device name: Fluido® Pressure Chamber
Device model: 660300
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: The Surgical Company International B.V.
SRN: NL-MF-000001973
Country: Netherlands
Email: raqa.ptm@tsc-life.com
Phone: +31207902100

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KJWND84C7A7V7QPFEKDCWWSZ

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

66030018719867001622