Identity
- Trade Name
- SURFLASH FDA UDI
- Generic Name
- Peripheral intravenous cannula FDA UDI
- Device Name
- SURFLASH I.V. catheter FDA UDI
- Model / Reference
- SR*FF1851 FDA UDI
- Description
- SURFLASH I.V. catheter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 34987350747915 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Peripheral intravenous cannula FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Length — 2 Inch FDA UDI
Category: Peripheral intravenous cannula
Surflash by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peripheral intravenous cannula.
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
- Supercath 5 — TOGO MEDIKIT CO., LTD. · Class II
- Nipro SafeTouch IV Catheter — NIPRO MEDICAL CORPORATION · Class II
- BioFlo — NAVILYST MEDICAL, INC. · Class II
- Navilyst Medical — NAVILYST MEDICAL, INC.
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
- Navilyst Medical — NAVILYST MEDICAL, INC.
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
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
- Terumo Corp.
Sources (1)
- FDA UDI 7a58c721-bc2c-4577-a2c2-7041fbc4e418 36 fields · synced Jun 8, 2026