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Centurion

FDA UDI

Class II (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Peripheral intravenous catheterization support kit FDA UDI
Device Name
PORT ACCESS KIT FDA UDI
Model / Reference
DT22575C FDA UDI
Description
PORT ACCESS KIT FDA UDI

Identifiers

Catalog Number
DT22575C FDA UDI
Primary DI / UDI-DI
10653160368137 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Peripheral intravenous catheterization support kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

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 catheterization support kit

Centurion by Centurion Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous catheterization support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c44a3e8d-fc6d-4f66-8b51-0ed675f98a04 35 fields · synced May 30, 2026