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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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MD Atlas
PAUL HARTMANN AG

Data from EUDAMED, last updated May 31, 2026

3212

40495003212K6

1 reference

Class I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk category: Class I
Manufacturer: PAUL HARTMANN AG

Device family identification

Device name: —
Basic UDI-DI: 40495003212K6
Device model: 3212
Issuing agency: GS1
Version date: May 27, 2026

Classification

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk category: Class I
Status: On the market

Manufacturer

Manufacturer

Name: PAUL HARTMANN AG
SRN: DE-MF-000005861
Country: Germany
Email: phag-eudamed@hartmann.info

Device characteristics

No device characteristics flagged

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

T04010201Untuckable underpads

References by status

References

1 reference

Export results

Applied filters

basicUdiUlid01KSMYEQY6VPKS5THHB12WKXAM

Format

Summary

31 columns included

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
161016	`161016`	`04052199738451`	30	On the market