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Secalon T 16g/1.70 X 160mm Mult=25/250

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
SECALON T 16G/1.70 X 160MM MULT=25/250 FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Catheter 16G/1.70x160mm & Pre Puncture Stylet Stabiliser FDA UDI
Model / Reference
681004 FDA UDI
Description
Catheter 16G/1.70x160mm & Pre Puncture Stylet Stabiliser FDA UDI

Identifiers

Catalog Number
681004 FDA UDI
Primary DI / UDI-DI
00886333610044 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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: Vascular catheter introduction set, nonimplantable

Secalon T 16g/1.70 X 160mm Mult=25/250 by Argon Critical Care Systems Singapore Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argon Critical Care Systems Singapore Pte. Ltd.

Sources (1)

  • FDA UDI 24f87d96-6abf-4a7c-bc4e-b644e60623bc 36 fields · synced May 31, 2026