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Connecta™ Pe Line M/F 75cm 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/F 75CM INT VOL 1.4ML/M FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Device Name
Male / Female Fittings PE line with tubing length 75cm FDA UDI
Model / Reference
682187 FDA UDI
Description
Male / Female Fittings PE line with tubing length 75cm FDA UDI

Identifiers

Catalog Number
682187 FDA UDI
Primary DI / UDI-DI
00886333621873 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/F 75cm 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

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Manufacturer

Sources (1)

  • FDA UDI 80f80d8b-093a-415a-a1c3-b61b5080c44e 36 fields · synced Jun 1, 2026