Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Centrally-inserted central venous catheter FDA UDI
- Device Name
- Single-Lumen Infusion Catheter (SLIC(R)) for use with Arrow Percutaneous Sheath Introducer System FDA UDI
- Model / Reference
- IPN055077 FDA UDI
- Description
- Single-Lumen Infusion Catheter (SLIC(R)) for use with Arrow Percutaneous Sheath Introducer System FDA UDI
Identifiers
- Catalog Number
- SS-14701 FDA UDI
- Primary DI / UDI-DI
- 10801902152852 FDA UDI
- FDA Product Code
- DYB FDA UDI
- GMDN Term
- Centrally-inserted central venous catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1340 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Category: Centrally-inserted central venous catheter
Arrow by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Centrally-inserted central venous catheter.
- Cook — COOK INCORPORATED · Class II
- Groshong — Bard Access Systems, Inc. · Class II
- Groshong — Bard Access Systems, Inc. · Class II
- Infusion Catheter — MEDICAL COMPONENTS INC · Class II
- VYGON — VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG · Class II
- VYGON — VYGON-Erzeugnisse für Medizin und Chirurgie-GmbH und Co. KG · Class II
- Hickman TriFusion — Bard Access Systems, Inc. · Class II
- PowerHickman — Bard Access Systems, 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
- Teleflex Incorporated
Sources (1)
- FDA UDI 1e70bf7e-eb73-493d-826a-7b4a14752a8d 35 fields · synced May 29, 2026