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Procleix Assay Fluids Kit

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 303344

by Grifols Diagnostic Solutions Inc.

Identity

Trade Name
Procleix Assay Fluids Kit EUDAMED
Procleix Panther Lower Bay Fluids FDA UDI
Generic Name
Nucleic acid technique (NAT) kit IVD FDA UDI
Device Name
Procleix Assay Fluids Kit EUDAMED
A collection of reagents and other associated materials intended to be used to optimize an assay performed using a nucleic acid technique (NAT) on a clinical specimen. FDA UDI
Model / Reference
303344 EUDAMED
Procleix Assay Fluids FDA UDI
Description
A collection of reagents and other associated materials intended to be used to optimize an assay performed using a nucleic acid technique (NAT) on a clinical specimen. FDA UDI

Identifiers

Primary DI / UDI-DI
00859882007610 EUDAMEDFDA UDI
Basic UDI-DI
0859882007Procleix011ZD EUDAMED
Direct Marketing DI
00859882007610 EUDAMED
EMDN Code
W01019001 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (CC) EUDAMED
GMDN Term
Nucleic acid technique (NAT) kit IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Procleix Assay Fluids Kit by Grifols Diagnostic Solutions Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000004304
Authorised Representative
Diagnostic Grifols, S.A. ES-AR-000001573

Sources (2)

  • EUDAMED b0f85597-1c8a-4b8d-9321-faeb499aa1d7 61 fields · synced Jun 19, 2026
  • FDA UDI 9cc7a50e-0523-4bfa-99c2-fae5670125cd 33 fields · synced May 30, 2026