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Syva® Emit® 2000 Digoxin Calibrators

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Syva® Emit® 2000 Digoxin Calibrators FDA UDI
Generic Name
Digoxin therapeutic drug monitoring IVD, calibrator FDA UDI
Device Name
Emit ® 2000 Digoxin Calibrators FDA UDI
Model / Reference
10445316 FDA UDI
Description
Emit ® 2000 Digoxin Calibrators FDA UDI

Identifiers

Catalog Number
4H209UL FDA UDI
Primary DI / UDI-DI
00842768000973 FDA UDI
510(k) Number
K934135 FDA UDI
FDA Product Code
KXT FDA UDI
GMDN Term
Digoxin therapeutic drug monitoring IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3320 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: Digoxin therapeutic drug monitoring IVD, calibrator

Syva® Emit® 2000 Digoxin Calibrators by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Digoxin therapeutic drug monitoring IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare Diagnostics

Sources (1)

  • FDA UDI e3a73df3-52c8-484e-ada3-b556882a19d0 37 fields · synced May 30, 2026