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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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MEMOBAG — 3 UDI-DI variants, MDR (Teleflex Medical)

MD Atlas
Teleflex Medical

Data from EUDAMED, last updated May 24, 2026

MEMOBAG

08019020000000000000262KQ

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Teleflex Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08019020000000000000262KQ
Device name: MEMOBAG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Teleflex Medical
SRN: IE-MF-000015868
Country: Ireland
Email: orders.intl@teleflex.com
Phone: 353 (0) 9 06 46 08 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KPTVFKGJBW692MWWZSF3FP5X

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

MemoBag extraction bag, for 10 mm trocars, volume 1200 ml44026704760686
MemoBag extraction bag, for 10 mm trocars, volume 200 ml44026704760709
MemoBag extraction bag, for 10 mm trocars, volume 800 ml44026704760693