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Reagent Kit

FDA UDI

Class I (US FDA UDI)

by Chromsystems Instruments & Chemicals GmbH

Identity

Trade Name
Reagent Kit FDA UDI
Generic Name
HVA/VMA/5HIAA IVD, kit, liquid chromatography FDA UDI
Device Name
HPLC Reagent Kit, VMA, HVA, 5-HIAA in urine FDA UDI
Model / Reference
1000/B FDA UDI
Description
HPLC Reagent Kit, VMA, HVA, 5-HIAA in urine FDA UDI

Identifiers

Catalog Number
1000/B FDA UDI
Primary DI / UDI-DI
04250317500069 FDA UDI
FDA Product Code
CDF FDA UDI
GMDN Term
HVA/VMA/5HIAA IVD, kit, liquid chromatography FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1795 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: HVA/VMA/5HIAA IVD, kit, liquid chromatography

Reagent Kit by Chromsystems Instruments & Chemicals GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as HVA/VMA/5HIAA IVD, kit, liquid chromatography.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Chromsystems Instruments & Chemicals GmbH

Sources (1)

  • FDA UDI 1f82cd4a-1304-4a5d-a2e2-be87b183da6d 36 fields · synced Jun 8, 2026