Identity
- Trade Name
- Laport EUDAMED
- Device Name
- N21-1010 EUDAMED
- Model / Reference
- N21-1010 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08806182210402 EUDAMED
- Basic UDI-DI
- B-08806182210402 EUDAMED
- EMDN Code
- K01010101 TROCAR STANDARD, SINGLE-USE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Laport by Sejong Medical Co., Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08806182210402 | Class IIa | Active |
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Manufacturer
- Manufacturer
- SEJONG MEDICAL Co., Ltd.
- EUDAMED SRN
- KR-MF-000020090
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED 13c3db5d-f7c5-41bc-a527-545bfafb8936 61 fields · synced May 22, 2026