← Back to catalogue

Medcomp Pro-Picc With Valve Technologymedcomp Pro-Picc With Valve Technology

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
MEDCOMP PRO-PICC WITH VALVE TECHNOLOGYMEDCOMP PRO-PICC WITH VALVE TECHNOLOGY FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
5F X 60CM SINGLE LUMEN5F X 60CM PRO-PICC®CT W/VALVE TECHNOLOGY BASIC IR SETTECHNOLOG FDA UDI
Model / Reference
MD82035101 FDA UDI
Description
5F X 60CM SINGLE LUMEN5F X 60CM PRO-PICC®CT W/VALVE TECHNOLOGY BASIC IR SETTECHNOLOG FDA UDI

Identifiers

Catalog Number
MD82035101 FDA UDI
Primary DI / UDI-DI
00884908137439 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

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

Medcomp Pro-Picc With Valve Technologymedcomp Pro-Picc With Valve Technology by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medical Components Inc

Sources (1)

  • FDA UDI 616dfea7-cd72-4264-a89d-b5c03771b733 35 fields · synced Jun 1, 2026