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Veress Needle
EUDAMEDFDA 510(k)Class IIa (EU MDR)
Ref WVN0115T
by WickiMed (HuiZhou) Medical Equipment Manufacturing Co., Ltd
Identity
- Trade Name
- Veress Needle EUDAMED
- Device Name
- Sterile single use veress needle EUDAMED
- Model / Reference
- WVN0115T EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970739457373 EUDAMED
- Basic UDI-DI
- 697073945TD008K2 EUDAMED
- Direct Marketing DI
- 06970739457373 EUDAMED
- EMDN Code
- K0104 VERESS NEEDLES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
Veress Needle by WickiMed (HuiZhou) Medical Equipment Manufacturing Co., Ltd — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA 510(k)
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K172120 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 697073945TD008K2 | Class IIa | Active |
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Manufacturer
- EUDAMED SRN
- CN-MF-000027477
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (2)
- EUDAMED 5a2be2e1-3d75-45cd-982c-1c60088d8752 61 fields · synced Jun 20, 2026
- FDA 510(k) K172120 1 fields · synced May 18, 2026