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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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IQ Dose — 4 UDI-DI variants, MDR (Stiplastics)

MD Atlas
Stiplastics

Data from EUDAMED, last updated May 19, 2026

IQ Dose

37011717IQDOSE01PS

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: Stiplastics

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 37011717IQDOSE01PS
Device name: IQ Dose
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 9, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J9RG8TN1DJNED5K036Y1K5VJ

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

STI202D 000A0103701171702348
STI202D 000F0003701171707251
STI202 00011003701171707534
STI202D 000B0003701171701082