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Genesis Rapid Seal Pro™ Tube Sealer
EUDAMEDClass I (EU MDR)
Ref 08809241444725Model SE7
Identity
- Trade Name
- GENESIS RAPID SEAL PRO™ TUBE SEALER EUDAMED
- Device Name
- TUBE SEALER EUDAMED
- Model / Reference
- SE7 EUDAMED08809241444725 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08809241444725 EUDAMED
- Basic UDI-DI
- 880924144CEN4725CG EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Genesis Rapid Seal Pro™ Tube Sealer by Centron Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 880924144CEN4725CG | Class I | Active |
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Manufacturer
- Manufacturer
- Centron Corporation
- EUDAMED SRN
- KR-MF-000050692
- Authorised Representative
- Globe Scientific Europe NL-AR-000050612
Sources (1)
- EUDAMED aceffcad-8b89-4469-b559-14a0610c729d 61 fields · synced Jun 20, 2026