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Autocheck 6+, Level 1, S7835

FDA UDI

Class I (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
AUTOCHECK 6+, LEVEL 1, S7835 FDA UDI
Generic Name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI
Device Name
S7835 AutoCheck 6+, level 1 box of 30 ampoules, for ABL8XX FDA UDI
Model / Reference
944-094 FDA UDI
Description
S7835 AutoCheck 6+, level 1 box of 30 ampoules, for ABL8XX FDA UDI

Identifiers

Catalog Number
944-094 FDA UDI
Primary DI / UDI-DI
05700699440945 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple blood gas/haemoximetry/electrolyte analyte IVD, control

Autocheck 6+, Level 1, S7835 by Radiometer Medical ApS — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple blood gas/haemoximetry/electrolyte analyte IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8ac9f384-88b4-4f7e-be69-aaf6e7e6cb95 36 fields · synced May 30, 2026