Identity
- Trade Name
- Probe EUDAMED
- Device Name
- Probe EUDAMED
- Model / Reference
- PBE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08964003662493 EUDAMED
- Basic UDI-DI
- 8964003662ProbeVG EUDAMED
- EMDN Code
- L031101 FISTULA PROBES, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Probe by CENTRAL SURGICAL Co. (PVT) LTD. — 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 | 8964003662ProbeVG | Class I | Active |
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Manufacturer
- Manufacturer
- CENTRAL SURGICAL Co. (PVT) LTD.
- EUDAMED SRN
- PK-MF-000035590
- Authorised Representative
- KHANG BAO INTERNATIONAL KFT HU-AR-000034102
Sources (1)
- EUDAMED ecd4895b-88d1-4d18-ae6a-b7539a8bb2dd 61 fields · synced Jun 19, 2026