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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 120CM SCHON GUIDEWIRE FDA UDI
- Model / Reference
- SCHON GW FDA UDI
- Description
- 0.035 (0.9MM) X 120CM SCHON GUIDEWIRE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908041125 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
A comprehensive medical device directory entry for CardioVascular Spring Guidescardiovascular Spring Guides, providing detailed information on its features, compliance, and FAQs.
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 |
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Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 08be2e61-4c66-485e-b00f-f72ccaea9bd6 35 fields · synced Jul 7, 2026