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Health Line

FDA UDI

Class II (US FDA UDI)

by Health Line International Corp

Identity

Trade Name
Health Line FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
Health Line 5F x 20cm Single Lumen CT Midline Nursing Kit FDA UDI
Model / Reference
A120-05120-N FDA UDI
Description
Health Line 5F x 20cm Single Lumen CT Midline Nursing Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00876604000766 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripherally-inserted central venous catheter 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

Yes

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: Peripherally-inserted central venous catheter

Health Line by Health Line International Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Health Line International Corp

Sources (1)

  • FDA UDI 8ff9a78b-a211-46d7-b066-07d66cb73ee9 33 fields · synced May 30, 2026