Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Intravascular ultrasound imaging catheter, single-use FDA UDI
- Device Name
- VPS G4(TM) Base Unit and Interface with Accessories-Refurbished FDA UDI
- Model / Reference
- IPN037703 FDA UDI
- Description
- VPS G4(TM) Base Unit and Interface with Accessories-Refurbished FDA UDI
Identifiers
- Catalog Number
- VPS-G4C-R FDA UDI
- Primary DI / UDI-DI
- 30801902130267 FDA UDI
- FDA Product Code
- OBJ FDA UDI
- GMDN Term
- Intravascular ultrasound imaging catheter, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Category: Intravascular ultrasound imaging catheter, single-use
Arrow by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular ultrasound imaging catheter, single-use.
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- Novasight Hybrid™ Catheter PIM Bag — Conavi Medical Inc · Class II
- OptiCross™ 6 — Boston Scientific · Class II
- OptiCross™ HD — Boston Scientific · 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
- Teleflex Incorporated
Sources (1)
- FDA UDI 81e0545c-6ba7-4be7-a1c1-6c64601e6a5c 35 fields · synced Jun 1, 2026