Sy12-Ltr

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name: SY12-LTR FDA UDI
Generic Name: Angiographic syringe FDA UDI
Device Name: 12ml with Male Luer Taper Syringe FDA UDI
Model / Reference: 682256 FDA UDI
Description: 12ml with Male Luer Taper Syringe FDA UDI

Identifiers

Catalog Number: 682256 FDA UDI
Primary DI / UDI-DI: 00886333622566 FDA UDI
FDA Product Code: DQF FDA UDI
GMDN Term: Angiographic syringe FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1670 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Angiographic syringe

Sy12-Ltr by Argon Critical Care Systems Singapore Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Argon Critical Care Systems Singapore Pte. Ltd.

Sources (1)

FDA UDI ad752f9d-0600-4044-be26-a7c2df0e465c 36 fields · synced Jun 8, 2026