← Back to catalogue

Syva® RapidTest d.a.u.® BZO

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Syva® RapidTest d.a.u.® BZO FDA UDI
Generic Name
Benzodiazepine group IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Syva® RapidTest d.a.u.® BZO, Benzodiazepines FDA UDI
Model / Reference
10445365 FDA UDI
Description
Syva® RapidTest d.a.u.® BZO, Benzodiazepines FDA UDI

Identifiers

Catalog Number
6A449UL FDA UDI
Primary DI / UDI-DI
00842768001369 FDA UDI
FDA Product Code
JXM FDA UDI
GMDN Term
Benzodiazepine group IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3170 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

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: Benzodiazepine group IVD, kit, rapid ICT, clinical

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

Similar devices

Also classified as Benzodiazepine group IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0ea7faf6-9290-4d0e-b852-f64183a12fe3 36 fields · synced May 30, 2026