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Whole Blood Calibration Standard

FDA UDI

Class II (US FDA UDI)

by Chromsystems Instruments & Chemicals GmbH

Identity

Trade Name
Whole Blood Calibration Standard FDA UDI
Generic Name
Glutathione IVD, kit, liquid chromatography FDA UDI
Device Name
Whole Blood Calibration Standard Glutathione FDA UDI
Model / Reference
66003 FDA UDI
Description
Whole Blood Calibration Standard Glutathione FDA UDI

Identifiers

Catalog Number
66003 FDA UDI
Primary DI / UDI-DI
04250317544070 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Glutathione IVD, kit, liquid chromatography FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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: Glutathione IVD, kit, liquid chromatography

Whole Blood Calibration Standard by Chromsystems Instruments & Chemicals GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a4214a7a-9739-4416-b077-086651dc462b 37 fields · synced May 30, 2026