Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Central venous catheterization kit, short-term FDA UDI
- Device Name
- Four-Lumen CVC FDA UDI
- Model / Reference
- IPN918560 FDA UDI
- Description
- Four-Lumen CVC FDA UDI
Identifiers
- Catalog Number
- CV-15854 FDA UDI
- Primary DI / UDI-DI
- 10801902181241 FDA UDI
- GMDN Term
- Central venous catheterization kit, short-term FDA UDI
Classification
- 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
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: Central venous catheterization kit, short-term
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 23254919-087c-4a93-8d68-04c88bd06e18 35 fields · synced May 30, 2026