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Non Vacuum Blood Collection Tube
EUDAMEDClass A (EU MDR)
Ref GLASSModel No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride
Identity
- Device Name
- Non Vacuum Blood Collection Tube EUDAMED
- Model / Reference
- No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride EUDAMEDGLASS EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06973905960400 EUDAMED
- Basic UDI-DI
- 697390596NVBCT018P EUDAMED
- EMDN Code
- W050101010201,W050101010202 EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
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
No
EUDAMED
New Device
No
EUDAMED
Non Vacuum Blood Collection Tube by Shandong Chengwu Medical Products Factory — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 697390596NVBCT018P | Class A | Active |
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Manufacturer
- Manufacturer
- Shandong Chengwu Medical Products Factory
- EUDAMED SRN
- CN-MF-000003370
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED 0e679c9e-0601-4c84-b731-1177335e41f8 61 fields · synced Oct 7, 2026