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EliReel

EUDAMED

Class I (EU MDR)

Ref 19500002Model 13735Ref 19500006Ref 19500005Ref 19500000

by W&H Sterilization Srl

Identity

Trade Name
EliReel EUDAMED
Device Name
EliReel EUDAMED
Model / Reference
13735 EUDAMED
19500002 EUDAMED
19500006 EUDAMED
19500005 EUDAMED
19500000 EUDAMED

Identifiers

Primary DI / UDI-DI
09010532026103 EUDAMED
09010532026141 EUDAMED
09010532026134 EUDAMED
09010532026080 EUDAMED
Basic UDI-DI
9010532137355Q EUDAMED
EMDN Code
S01020101 FLAT STERILISATION REELS, PAPER/PLASTIC FILM EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

EliReel by W&H Sterilization Srl — 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

EUDAMED SRN
IT-MF-000008237

Sources (4)

  • EUDAMED 04e00da2-ce1e-45e1-9954-ba786db964ef 61 fields · synced Jul 26, 2026
  • EUDAMED d46495cf-2892-4010-a70e-e1cda4060c73 61 fields · synced May 18, 2026
  • EUDAMED 8d7d7b28-ca3a-467f-b56a-71344f22e66c 61 fields · synced May 19, 2026
  • EUDAMED abe0d154-8bc8-4263-8db4-d2abdbccba2d 61 fields · synced May 19, 2026