Identity
- Trade Name
- CELLPACK DST FDA UDI
- Generic Name
- Buffered sample diluent IVD FDA UDI
- Device Name
- CELLPACK DST EUDAMEDCELLPACK DST is a concentrated diluent for use in Sysmex Automated Hematology Analyzers and other Sysmex devices that use diluted CELLPACK DST. CELLPACK DST must only be used with the Reagent Preparation Units specified by Sysmex. FDA UDI
- Model / Reference
- BM-808-974 EUDAMEDFDA UDI
- Description
- CELLPACK DST is a concentrated diluent for use in Sysmex Automated Hematology Analyzers and other Sysmex devices that use diluted CELLPACK DST. CELLPACK DST must only be used with the Reagent Preparation Units specified by Sysmex. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987562422944 EUDAMEDFDA UDI
- Basic UDI-DI
- 4987562CELLPACKDSTZ9 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 EUDAMEDClass 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 — 4 Liter FDA UDI
Cellpack Dst 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 4987562CELLPACKDSTZ9 | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Sysmex Corporation
- EUDAMED SRN
- JP-MF-000014037
- Authorised Representative
- Sysmex Europe SE DE-AR-000022333
Sources (2)
- EUDAMED 857132e0-d014-4f22-a2fb-b49b34ad626c 61 fields · synced Jun 8, 2026
- FDA UDI 55e378f8-41e2-45a7-b757-d4575b4bed16 36 fields · synced May 30, 2026