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Safedraw™

FDA UDI

Class II (US FDA UDI)

by Argon Critical Care Systems Singapore Pte. Ltd.

Identity

Trade Name
Safedraw™ FDA UDI
Generic Name
In-line arterial blood sampling set FDA UDI
Model / Reference
10884450384807 FDA UDI

Identifiers

Catalog Number
688695/B FDA UDI
Primary DI / UDI-DI
10884450384807 FDA UDI
FDA Product Code
DSK FDA UDI
GMDN Term
In-line arterial blood sampling set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1110 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

No

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: In-line arterial blood sampling set

Safedraw™ 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 In-line arterial blood sampling set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b930fdb-51a2-4bf8-bdcb-542af32da679 33 fields · synced May 30, 2026