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Bicarbonate Liquid

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Bicarbonate Liquid FDA UDI
Generic Name
Carbon dioxide (CO2) IVD, kit, spectrophotometry FDA UDI
Model / Reference
08057494190 FDA UDI

Identifiers

Catalog Number
08057494190 FDA UDI
Primary DI / UDI-DI
07613336121146 FDA UDI
510(k) Number
K031879 FDA UDI
FDA Product Code
KHS FDA UDI
GMDN Term
Carbon dioxide (CO2) IVD, kit, spectrophotometry 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

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

No

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: Carbon dioxide (CO2) IVD, kit, spectrophotometry

Bicarbonate Liquid by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide (CO2) IVD, kit, spectrophotometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96812c1f-1c2b-43ed-9c44-25b1d994eea7 35 fields · synced Jun 8, 2026