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Memorial Sloan Kettering Arterial Extension Set

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
MEMORIAL SLOAN KETTERING ARTERIAL EXTENSION SET FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Device Name
A 3-way white stopcock connects to a 12" presure tubing. It includes a separately packed 2x male protective caps. FDA UDI
Model / Reference
687201 FDA UDI
Description
A 3-way white stopcock connects to a 12" presure tubing. It includes a separately packed 2x male protective caps. FDA UDI

Identifiers

Catalog Number
687201 FDA UDI
Primary DI / UDI-DI
00886333672011 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Invasive blood pressure monitoring tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

Memorial Sloan Kettering Arterial Extension Set 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 9b3ba635-0762-404c-81f3-813c28de62dd 36 fields · synced May 31, 2026