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Careflow™

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
Careflow™ FDA UDI
Generic Name
Central venous catheterization kit, short-term FDA UDI
Model / Reference
10884450321895 FDA UDI

Identifiers

Catalog Number
681720/A FDA UDI
Primary DI / UDI-DI
10884450321895 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Central venous catheterization kit, short-term 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

No

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

A comprehensive medical device directory listing the Careflow™ device, including its features, regulatory compliance, and FAQs.

Similar devices

Also classified as Central venous catheterization kit, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a3e16cb-a842-4c84-bb0c-b5bf9fc3a550 34 fields · synced Jul 9, 2026