Identity
- Trade Name
- McKesson FDA UDI
- Generic Name
- Peripheral intravenous cannula FDA UDI
- Device Name
- Catheter, IV safety, push button, sterile, Yellow, Winged 24G x .75 in FDA UDI
- Model / Reference
- 192-PB2475W FDA UDI
- Description
- Catheter, IV safety, push button, sterile, Yellow, Winged 24G x .75 in FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10612479250212 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
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
Yes
FDA UDI
Category: Peripheral intravenous cannula
McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Peripheral intravenous cannula.
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- SURFLASH — Terumo Corp. · 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
- Mckesson Medical-Surgical Inc.
Sources (1)
- FDA UDI c21296b8-60f0-4917-a080-c159c72ae454 33 fields · synced May 30, 2026