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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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Inhalation Chamber — 8 UDI-DI variants, MDR (Stiplastics)

MD Atlas
Stiplastics

Data from EUDAMED, last updated May 19, 2026

Inhalation Chamber

37011717CHAMBRE01PE

8 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: Stiplastics

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 37011717CHAMBRE01PE
Device name: Inhalation Chamber
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: Stiplastics
SRN: FR-MF-000000826
Country: France
Email: regulatory@sgh-medical.com

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01HCYVS02M1SMN6W1042CZ609A

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

STI903D-S02 VIA00203701171707664
STI903D-L02 VIA00203701171707688
STI903D-M02 VIA00203701171707671
STI903D-M01 00000003701171700320
STI903D-S02 VIA00103701171707244
STI903D-M02 VIA00103701171707237
STI903D-S01 00000003701171700337
STI903D-L02 VIA00103701171707220