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Pro-Line® CT

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
Pro-Line® CT FDA UDI
Generic Name
Centrally-inserted central venous catheter FDA UDI
Device Name
6F X 60CM TRIPLE Pro-Line® CT OR SET W/0.038" WIRE FDA UDI
Model / Reference
MR28036304 FDA UDI
Description
6F X 60CM TRIPLE Pro-Line® CT OR SET W/0.038" WIRE FDA UDI

Identifiers

Primary DI / UDI-DI
00884908105056 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Centrally-inserted central venous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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: Centrally-inserted central venous catheter

Pro-Line® CT by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Centrally-inserted central venous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Components Inc

Sources (1)

  • FDA UDI ab1dbc0f-0a58-46e2-96bd-e59fc9ae662f 34 fields · synced Jun 6, 2026