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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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POCKET III — 1 UDI-DI variant, MDR (QUANTEL MEDICAL)

MD Atlas
QUANTEL MEDICAL

Data from EUDAMED, last updated May 31, 2026

POCKET III

37005426POCKETIIIBE

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: QUANTEL MEDICAL

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 37005426POCKETIIIBE
Device name: POCKET III
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: QUANTEL MEDICAL
SRN: FR-MF-000009724
Country: France
Email: eudamed@quantelmedical.fr

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSJ2128R8QQG7KKSGC2FAWJ9

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

POCKET III03700542626009