← Back to catalogue
Cardiovascular Spring Guidescardiovascular Spring Guides
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- CARDIOVASCULAR SPRING GUIDESCARDIOVASCULAR SPRING GUIDES FDA UDI
- Generic Name
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
- Device Name
- 0.035" (0.9MM) X 70CM GUIDEWIRE FDA UDI
- Model / Reference
- MC35 FDA UDI
- Description
- 0.035" (0.9MM) X 70CM GUIDEWIRE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908029215 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1330 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
No
FDA UDI
Cardiovascular Spring Guidescardiovascular Spring Guides by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 13305de0-2960-4942-a971-5e4df1194633 35 fields · synced May 31, 2026