← Back to catalogue

Connecta™ Pe Line M/M 100cm Int Vol 1.4ml/M

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
CONNECTA™ PE LINE M/M 100CM INT VOL 1.4ML/M FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Device Name
Male / Male Fittings PE line with tubing length 100cm FDA UDI
Model / Reference
682190 FDA UDI
Description
Male / Male Fittings PE line with tubing length 100cm FDA UDI

Identifiers

Catalog Number
682190 FDA UDI
Primary DI / UDI-DI
00886333621903 FDA UDI
FDA Product Code
FMG FDA UDI
GMDN Term
Invasive blood pressure monitoring tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

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: Invasive blood pressure monitoring tubing set

Connecta™ Pe Line M/M 100cm Int Vol 1.4ml/M by Argon Critical Care Systems Singapore Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Invasive blood pressure monitoring tubing set.

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

Sources (1)

  • FDA UDI 44d94989-65b9-4fd0-94ff-854a81464ef9 36 fields · synced Jun 1, 2026