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Cellodent

EUDAMED

Class I (EU MDR)

Ref 263010Model 1006Ref 263030

by Ivf Hartmann Ag

Identity

Trade Name
Cellodent EUDAMED
Device Name
Cellodent swabs EUDAMED
Model / Reference
1006 EUDAMED
263010 EUDAMED
263030 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600263011 EUDAMED
07611600953240 EUDAMED
Basic UDI-DI
76116001006LJ EUDAMED
Unit of Use DI
07611600996780 EUDAMED
07611600996773 EUDAMED
EMDN Code
M020299 NON-WOVEN GAUZES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Cellodent by Ivf Hartmann Ag — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Ivf Hartmann Ag
EUDAMED SRN
CH-MF-000015962
Authorised Representative
PAUL HARTMANN AG DE-AR-000007519

Sources (2)

  • EUDAMED 50f6d7cb-0bb7-4fad-a432-ad10f8e9d19e 61 fields · synced Oct 6, 2026
  • EUDAMED 588de606-8c96-437c-9f27-0f260be7eca1 61 fields · synced May 19, 2026