Identity
- Trade Name
- SURFLASH FDA UDI
- Generic Name
- Peripheral vascular catheter FDA UDI
- Device Name
- SURFLASH safety I.V. catheter FDA UDI
- Model / Reference
- SR*FNP1451 FDA UDI
- Description
- SURFLASH safety I.V. catheter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 34987350724824 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Peripheral vascular catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 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
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
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 2 Inch FDA UDI
Surflash by Terumo Corp. — 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
- Terumo Corp.
Sources (1)
- FDA UDI e3693e62-274f-4608-82e1-276d90ec1aa7 37 fields · synced Jun 1, 2026