← Back to catalogue

Fosforo UV

EUDAMED

Class IVD General (EU MDR)

Ref 0039Ref 0031

by Giesse Diagnostics Srl

Identity

Trade Name: Fosforo UV EUDAMED
Device Name: Fosforo UV/Phosphorus UV EUDAMED
Model / Reference: 0039 EUDAMED
0031 EUDAMED

Identifiers

Primary DI / UDI-DI: 08053172970789 EUDAMED
08053172970772 EUDAMED
Basic UDI-DI: B-08053172970789 EUDAMED
B-08053172970772 EUDAMED
EMDN Code: W01010307 PHOSPHATE INORGANIC / PHOSPHORUS EUDAMED

Classification

Device Class: Class IVD General EUDAMED
Market of Registration: Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Category: Inorganic phosphate (PO43-) IVD, reagent

Fosforo UV by Giesse Diagnostics Srl — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Inorganic phosphate (PO43-) IVD, reagent.

BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
Phosphorus UV, 2 x 100 mL — Chronolab Systems, S.L. · IVD General
Liquick Cor-PHOSPHORUS 30 — PZ CORMAY Spółka Akcyjna · IVD General
BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
Pointe Scientific, Inc. Phosphorus — POINTE SCIENTIFIC, INC. · Class I
ACCENT-300 PHOSPHORUS — PZ CORMAY Spółka Akcyjna · IVD General
Alinity — Abbott · Class I
OS-PHOSPHORUS — PZ CORMAY Spółka Akcyjna · IVD General

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Giesse Diagnostics Srl
EUDAMED SRN: IT-MF-000039031

Sources (2)

EUDAMED 66d99860-6afa-4b97-9941-71d80fb2524e 61 fields · synced Jul 21, 2026
EUDAMED 0dde4c46-0505-4c45-996e-338086d536de 61 fields · synced May 18, 2026