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Sicu Anesthesia Set

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
SICU ANESTHESIA SET FDA UDI
Generic Name
Invasive blood pressure monitoring tubing set FDA UDI
Device Name
A single 3cc transducer connected to a 20 drops, 60" tube Adset. The patient line is connected with a 48" pressure tube and a 12" pressure tube via 3-way White stopcocks. FDA UDI
Model / Reference
687100 FDA UDI
Description
A single 3cc transducer connected to a 20 drops, 60" tube Adset. The patient line is connected with a 48" pressure tube and a 12" pressure tube via 3-way White stopcocks. FDA UDI

Identifiers

Catalog Number
687100 FDA UDI
Primary DI / UDI-DI
00886333671007 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

Sicu Anesthesia Set by Argon Critical Care Systems Singapore Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 b9819013-d630-419f-9b35-756123124219 36 fields · synced May 30, 2026