Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Peripheral intravenous cannula FDA UDI
- Device Name
- ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System FDA UDI
- Model / Reference
- IPN927499 FDA UDI
- Description
- ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System FDA UDI
Identifiers
- Catalog Number
- EDC-00620-M FDA UDI
- Primary DI / UDI-DI
- 10801902214130 FDA UDI
- 510(k) Number
- K163513 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
Yes
FDA UDI
Combination Product
Yes
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: Peripheral intravenous cannula
Arrow by Teleflex Incorporated — 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
Cleared under the same submission
K163513 also covers:
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
- ARROW — TELEFLEX INCORPORATED
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
- Teleflex Incorporated
Sources (1)
- FDA UDI 18998013-312b-440b-ad4b-de715ccac5df 37 fields · synced Jun 8, 2026