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ABX Basolyse 5L

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 0204050

by Horiba Abx Sas

Identity

Trade Name
ABX Basolyse 5L EUDAMED
ABX BASOLYSE FDA UDI
Generic Name
Blood cell lysis reagent IVD FDA UDI
Device Name
ABX Basolyse 5L EUDAMED
Model / Reference
0204050 EUDAMED
1210204050 FDA UDI

Identifiers

Primary DI / UDI-DI
03610230004425 EUDAMEDFDA UDI
Basic UDI-DI
361023basolyse_5LC8 EUDAMED
Direct Marketing DI
03610230004425 EUDAMED
FDA Product Code
GGK FDA UDI
EMDN Code
W0103010103 COMPLETE CELL COUNT EUDAMED
GMDN Term
Blood cell lysis reagent IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.8540 FDA UDI
Market of Registration
France 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

ABX Basolyse 5L by Horiba Abx Sas — 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

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Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (2)

  • EUDAMED 5ed21f27-c118-4162-ab20-8f9567755654 61 fields · synced Jul 12, 2026
  • FDA UDI cbefd2d0-af3b-45c5-8360-68e958da6ae3 32 fields · synced May 30, 2026