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Syntel® Silicone Embolectomy Catheter - Regular Tip
EUDAMEDClass IIa (EU MDR)
Ref 1801-34M
Identity
- Trade Name
- Syntel® Silicone Embolectomy Catheter - Regular Tip EUDAMED
- Device Name
- Syntel® Silicone Embolectomy Catheter - Regular Tip EUDAMED
- Model / Reference
- 1801-34M EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00840663111756 EUDAMED
- Basic UDI-DI
- 08406631SyntelRTST EUDAMED
- EMDN Code
- C019002 EMBOLECTOMY CATHETERS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany 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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Syntel® Silicone Embolectomy Catheter - Regular Tip by LeMaitre Vascular, Inc. — Class IIa — 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 | 08406631SyntelRTST | Class IIa | Active |
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Manufacturer
- Manufacturer
- LeMaitre Vascular, Inc.
- EUDAMED SRN
- US-MF-000016778
- Authorised Representative
- LeMaitre Vascular GmbH DE-AR-000013539
Sources (1)
- EUDAMED 359f70d3-662c-45b3-9df4-b5ff3159d7c4 61 fields · synced Jun 18, 2026