Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Centrally-inserted central venous catheter FDA UDI
- Device Name
- Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter FDA UDI
- Model / Reference
- IPN914885 FDA UDI
- Description
- Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter FDA UDI
Identifiers
- Catalog Number
- CS-12802 FDA UDI
- Primary DI / UDI-DI
- 10801902159257 FDA UDI
- GMDN Term
- Centrally-inserted central venous catheter FDA UDI
Classification
- 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
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: Centrally-inserted central venous catheter
Arrow by Teleflex Incorporated — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 129295a4-aed8-4017-bf1c-b1bd5c718c7a 35 fields · synced May 31, 2026