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Cable Checker Tca-003

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
CABLE CHECKER TCA-003 FDA UDI
Generic Name
Pneumatic line tester, battery-powered FDA UDI
Device Name
A reusable device to verify the condition of an interface cable. FDA UDI
Model / Reference
684003 FDA UDI
Description
A reusable device to verify the condition of an interface cable. FDA UDI

Identifiers

Catalog Number
684003 FDA UDI
Primary DI / UDI-DI
00886333640034 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Pneumatic line tester, battery-powered 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pneumatic line tester, battery-powered

Cable Checker Tca-003 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 Pneumatic line tester, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 943157d8-8c26-4f81-902f-883548a79110 35 fields · synced May 30, 2026