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Syva® Emit® d.a.u.® Amphetamine Class Assay

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Syva® Emit® d.a.u.® Amphetamine Class Assay FDA UDI
Generic Name
Amphetamine/methamphetamine group IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Syva® Emit ® d.a.u.® Amphetamine Class Assay FDA UDI
Model / Reference
10445253 FDA UDI
Description
Syva® Emit ® d.a.u.® Amphetamine Class Assay FDA UDI

Identifiers

Catalog Number
3C019UL FDA UDI
Primary DI / UDI-DI
00842768017148 FDA UDI
510(k) Number
K900995 FDA UDI
FDA Product Code
DKZ FDA UDI
GMDN Term
Amphetamine/methamphetamine group IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3100 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

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: Amphetamine/methamphetamine group IVD, kit, enzyme immunoassay (EIA)

Syva® Emit® d.a.u.® Amphetamine Class Assay by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amphetamine/methamphetamine group IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae9b0ace-c848-41b7-ae4b-09c61fb5e724 37 fields · synced May 30, 2026