Identity
- Trade Name
- QBC Diagnostics FDA UDI
- Generic Name
- Full blood count IVD, kit, cell count FDA UDI
- Device Name
- QBC STAR, Refurbished EUDAMEDRefurbished QBC STAR-M Centrifugal Hematology System: Refurbished QBC STAR-M Analyzer; QBC Disposable Starter Kit (20 STAR Tubes) FDA UDI
- Model / Reference
- 42900109 EUDAMEDFDA UDI
- Description
- Refurbished QBC STAR-M Centrifugal Hematology System: Refurbished QBC STAR-M Analyzer; QBC Disposable Starter Kit (20 STAR Tubes) FDA UDI
Identifiers
- Catalog Number
- 42900109 FDA UDI
- Primary DI / UDI-DI
- 00858092006055 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00858092006055 EUDAMED
- 510(k) Number
- K992849 FDA UDI
- FDA Product Code
- GKZ FDA UDI
- EMDN Code
- W0202010101 AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr) EUDAMED
- GMDN Term
- Full blood count IVD, kit, cell count FDA UDI
Classification
- Device Class
- Class IVD General EUDAMEDClass II FDA UDI
- Regulation Number
- 864.5220 FDA UDI
- Market of Registration
- Northern Ireland 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
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
Yes
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
QBC STAR, Refurbished by Drucker Diagnostics — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-00858092006055 | Class IVD General | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IVD General | Pending data |
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Manufacturer
- Manufacturer
- Drucker Diagnostics
- EUDAMED SRN
- US-MF-000031517
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 158e02a6-c430-46da-b2a4-468aababba78 61 fields · synced Jun 18, 2026
- FDA UDI 077aabfb-5a19-4cc0-bea3-d42f8335a7de 35 fields · synced May 30, 2026