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Synermed®

FDA UDI

Class II (US FDA UDI)

by Infrared Laboratory Systems Llc

Identity

Trade Name
Synermed® FDA UDI
Generic Name
Multiple-type clinical chemistry analyte profile IVD, calibrator FDA UDI
Device Name
Drugs of Abuse Intermediate Calibrator 1 X 15 mL FDA UDI
Model / Reference
0854 FDA UDI
Description
Drugs of Abuse Intermediate Calibrator 1 X 15 mL FDA UDI

Identifiers

Catalog Number
0854 FDA UDI
Primary DI / UDI-DI
05060500091644 FDA UDI
510(k) Number
K133710 FDA UDI
FDA Product Code
DKB FDA UDI
GMDN Term
Multiple-type clinical chemistry analyte profile IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3200 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

Yes

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-type clinical chemistry analyte profile IVD, calibrator

Synermed® by Infrared Laboratory Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type clinical chemistry analyte profile IVD, calibrator.

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 741562d9-800d-4850-b592-804a1dbb90fa 37 fields · synced Jun 1, 2026