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Midline Catheter

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
Midline Catheter FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
4F X 20CM DUAL MIDLINE FULL NURSING KIT W/MAX BARRIER FDA UDI
Model / Reference
ML4D20MB FDA UDI
Description
4F X 20CM DUAL MIDLINE FULL NURSING KIT W/MAX BARRIER FDA UDI

Identifiers

Primary DI / UDI-DI
00884908096422 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Peripherally-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

Yes

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

Midline Catheter by Medical Components Inc — 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
Medical Components Inc

Sources (1)

  • FDA UDI f31547a0-8b13-4c10-83fe-87ee82267b29 34 fields · synced May 30, 2026