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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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Suction Tubes — 15 UDI-DI variants, MDR (Medica Europe B.V.)

MD Atlas
Medica Europe B.V.

Data from EUDAMED, last updated May 30, 2026

Suction Tubes

8710685TF01004001PE

15 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: Medica Europe B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8710685TF01004001PE
Device name: Suction Tubes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 4, 2023

Manufacturer & authorised representative

Manufacturer

Name: Medica Europe B.V.
SRN: NL-MF-000000118
Country: Netherlands
Email: qa@medica-europe.nl

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01GNYK9TA5W42VDZJ6KFKD96VX

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

120802AA08710685141616
120852AA08710685142224
260396008710685106530
230A74308710685106332
230A70108710685106295
230A87308710685106479
230A87508710685106493
230A75908710685106356
230A86608710685106394
230A86808710685106417
230A71208710685106318
230A76808710685106370
230A87108710685106431
230A87208710685106455
230A89508710685106516