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SSPC Delivery Catheter
EUDAMEDFDA UDIFDA 510(k)Class III (EU MDR)
Ref 9181Model SSPC1 (9181)Ref 9182
Identity
- Trade Name
- SSPC Delivery Catheter EUDAMEDSSPC1 Delivery Catheter FDA UDISSPC2 Delivery Catheter FDA UDI
- Generic Name
- Pacing/defibrillation lead delivery catheter FDA UDI
- Device Name
- SSPC Delivery Catheter EUDAMEDCatheter and Dilator FDA UDI
- Model / Reference
- SSPC1 (9181) EUDAMED9181 EUDAMEDFDA UDI9182 EUDAMEDFDA UDI
- Description
- Catheter and Dilator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810024670017 EUDAMED00810024670024 EUDAMED00810024671816 FDA UDI00810024671823 FDA UDI
- Basic UDI-DI
- B-00810024670017 EUDAMEDB-00810024670024 EUDAMED
- 510(k) Number
- K190475 FDA UDI
- FDA Product Code
- DQY FDA UDI
- EMDN Code
- C0502 CARDIOVASCULAR INTRODUCER SHEATHS, VALVED EUDAMED
- GMDN Term
- Pacing/defibrillation lead delivery catheter FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1250 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Catheter Working Length — 40 Centimeter FDA UDI
SSPC Delivery Catheter by CenterPoint Systems LLC — Class III — FDA_510K, MDD — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K190475 | Class III | Active |
| EUDAMED | European Union | CE/MDD | B-00810024670017 | Class III | Active |
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Manufacturer
- Manufacturer
- CenterPoint Systems LLC
- EUDAMED SRN
- US-MF-000009054
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (5)
- EUDAMED e1d6b430-2170-475b-981c-015d429206fd 61 fields · synced Sep 18, 2026
- FDA UDI 3054f6c4-02b5-4a06-b6a6-967d7549ff61 37 fields · synced May 29, 2026
- FDA UDI 3393ac39-f7b0-40c2-ba76-5651d2fe9838 37 fields · synced May 30, 2026
- EUDAMED f17c84ff-f437-46c8-a18c-a30cd5c348fe 61 fields · synced Sep 18, 2026
- FDA 510(k) K190475 1 fields · synced May 18, 2026