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Sy10-Rpr

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
SY10-RPR FDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
10 mL with Male Luer Taper syringe FDA UDI
Model / Reference
682250 FDA UDI
Description
10 mL with Male Luer Taper syringe FDA UDI

Identifiers

Catalog Number
682250 FDA UDI
Primary DI / UDI-DI
00886333622504 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

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: Angiographic syringe

Sy10-Rpr 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 Angiographic syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a53d7a2-80fe-4088-8271-5d7efafd578c 36 fields · synced May 30, 2026