← Back to catalogue

Cellpack Dcl

EUDAMEDFDA UDI

Class A (EU MDR)

Ref CT-661-628

by Sysmex Corporation

Identity

Trade Name
CELLPACK DCL EUDAMEDFDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
CELLPACK DCL EUDAMED
A reagent for measuring the numbers and sizes of RBC and platelets by the hydro dynamic focusing (DC Detection). FDA UDI
Model / Reference
CT-661-628 EUDAMED
CT661628 FDA UDI
Description
A reagent for measuring the numbers and sizes of RBC and platelets by the hydro dynamic focusing (DC Detection). FDA UDI

Identifiers

Primary DI / UDI-DI
04987562422906 EUDAMEDFDA UDI
Basic UDI-DI
4987562CELLPACKDCLX9 EUDAMED
FDA Product Code
GIF FDA UDI
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.8200 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

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

Dimensions & Sizes

Size
Total Volume — 20 Liter FDA UDI

Cellpack Dcl by Sysmex Corporation — 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

Manufacturer
Sysmex Corporation
EUDAMED SRN
JP-MF-000014037
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (2)

  • EUDAMED dc079c60-471b-4dc6-aa2d-6d604120c6d0 61 fields · synced Jul 25, 2026
  • FDA UDI 375a2cc2-eee2-4400-9c04-528840e6b8db 36 fields · synced May 30, 2026