Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Peripheral intravenous catheterization kit, non-sensing FDA UDI
- Device Name
- Pressure Injectable Two-Lumen Midline FDA UDI
- Model / Reference
- IPN923010 FDA UDI
- Description
- Pressure Injectable Two-Lumen Midline FDA UDI
Identifiers
- Catalog Number
- CDC-32052-MPKB FDA UDI
- Primary DI / UDI-DI
- 10801902205404 FDA UDI
- GMDN Term
- Peripheral intravenous catheterization kit, non-sensing 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
Yes
FDA UDI
MR Safe FDA UDI
Category: Peripheral intravenous catheterization kit, non-sensing
Arrow by Teleflex Incorporated — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peripheral intravenous catheterization kit, non-sensing.
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- V-Cath — Neo Medical Inc. · Class II
- V-Cath — Neo Medical Inc. · Class II
- NAR Kit — NORTH AMERICAN RESCUE, LLC. · 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 9458767c-66cb-445f-b7c4-5ba6d1e223f4 36 fields · synced Jun 8, 2026