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Vascu Puncture Picc Guidewirevascu Puncture Picc Guidewire
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- VASCU PUNCTURE PICC GUIDEWIREVASCU PUNCTURE PICC GUIDEWIRE FDA UDI
- Generic Name
- Peripheral vascular guidewire, manual FDA UDI
- Device Name
- 0.016" (0.4MM) X 130CM MARKED NITINOL GUIDEWIRE WITH RADIOPAQUE TIP FDA UDI
- Model / Reference
- MR190160 FDA UDI
- Description
- 0.016" (0.4MM) X 130CM MARKED NITINOL GUIDEWIRE WITH RADIOPAQUE TIP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908089745 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Peripheral vascular guidewire, manual 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
Vascu Puncture Picc Guidewirevascu Puncture Picc Guidewire 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 |
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Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 8b738442-016b-4bb7-bb2f-4e863ab8d07e 35 fields · synced May 30, 2026