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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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Zgłębnik — 13 UDI-DI variants, MDR (T.P.H. Pol-Intech Sp. z o.o.)

MD Atlas
T.P.H. Pol-Intech Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Zgłębnik

5903864742EXPLCU

13 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: T.P.H. Pol-Intech Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5903864742EXPLCU
Device name: —
Device model: Zgłębnik
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: T.P.H. Pol-Intech Sp. z o.o.
SRN: PL-MF-000007168
Country: Poland
Email: info@pol-intech.pl
Phone: +48 42 684 64 78

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2BTXC49NAH07MCTESEPJEV3

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

2139-0105903864742367
2139-0205903864742374
2139-0305903864742381
2139-0405903864742398
1198-00105903864742329
1198-00205903864742336
1198-00305903864742343
1198-00405903864742350
0274-00105903864742275
0274-00205903864742282
0274-00305903864742299
0274-00405903864742305
0274-00605903864742312