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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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HYPERTONIC SEA WATER — 51 UDI-DI variants, MDR

MD Atlas
STE PHARMACEUTICALS, S.L.U

Data from EUDAMED, last updated May 23, 2026

HYPERTONIC SEA WATER

843654262PL00338M

51 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: STE PHARMACEUTICALS, S.L.U

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UDI-DI variants

51 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9Q8A0ZKPKT2QVHTSJEDZ7F

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

PL0033_120_Soft08436617645181
PL0033_120_Medium08436617641565
PL0033_AD08436617641701
PL0033_AD08595566424893
PL0033_AD08595566424534
PL0033_120_Soft08595566422042
PL0033_AD08436542623827
PL0033_50_Medium08436617646850
PL0033_120_Soft08436542624152
PL0033_120_Strong08436542624183
PL0033_120_Medium08436542624176
PL0033_50_Strong08436617646898
PL0033_BB08436617640346
PL0033_100_Medium08436617643484
PL0033_100_Strong08436617643521
PL0033_100_Soft08436617643446
PL0033_50_Soft08436617646812
PL0033_120_Strong05202888106149
PL0033_120_Soft05202888106125
PL0033_120_Medium05202888106132
PL0033_120_Medium08470001788658
PL0033_50_Strong08436617646911
PL0033_120_Medium08436542621588
PL0033_100_Soft08436617643460
PL0033_AD08436542621946

1 2 3

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843654262PL00338M
Device name: HYPERTONIC SEA WATER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: STE PHARMACEUTICALS, S.L.U
SRN: ES-MF-000000144
Country: Spain
Email: ihernandez@stepharmaceuticals.com
Phone: +34 935923100

Variants by status