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JAS Diagnostics

FDA UDI

Class II (US FDA UDI)

by Drew Scientific , Ltd.

Identity

Trade Name
JAS Diagnostics FDA UDI
Generic Name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, kit, multiple technologies FDA UDI
Device Name
CARBON DIOXIDE LIQUID 405nm (6x 20mL) FDA UDI
Model / Reference
XL-CO23-20 FDA UDI
Description
CARBON DIOXIDE LIQUID 405nm (6x 20mL) FDA UDI

Identifiers

Primary DI / UDI-DI
00817274021118 FDA UDI
FDA Product Code
KHS FDA UDI
GMDN Term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, kit, multiple technologies FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1160 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple blood gas/haemoximetry/electrolyte analyte IVD, kit, multiple technologies

JAS Diagnostics by Drew Scientific , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple blood gas/haemoximetry/electrolyte analyte IVD, kit, multiple technologies.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76fdd394-1b19-439e-ba66-f91f804d79f7 35 fields · synced Jun 8, 2026