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Syva® Emit® II Plus Specialty Drug Control Negative

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Syva® Emit® II Plus Specialty Drug Control Negative FDA UDI
Generic Name
Multiple drugs of abuse IVD, control FDA UDI
Device Name
Syva® Emit® II Plus Buprenorphine Control Negative FDA UDI
Model / Reference
10718700 FDA UDI
Description
Syva® Emit® II Plus Buprenorphine Control Negative FDA UDI

Identifiers

Catalog Number
9S609UL FDA UDI
Primary DI / UDI-DI
00630414601083 FDA UDI
510(k) Number
K150606 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Multiple drugs of abuse IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 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: Multiple drugs of abuse IVD, control

Syva® Emit® II Plus Specialty Drug Control Negative by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple drugs of abuse IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd1ea8dd-d56e-4fdd-80ca-f398fa84e0ff 37 fields · synced Jun 8, 2026