← Back to catalogue

Synermed®

FDA UDI

Class I (US FDA UDI)

by Infrared Laboratory Systems Llc

Identity

Trade Name
Synermed® FDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Device Name
Automated Clinical Chemistry Analyzer IVD FDA UDI
Model / Reference
IR-1200 FDA UDI
Description
Automated Clinical Chemistry Analyzer IVD FDA UDI

Identifiers

Catalog Number
IR-1200 FDA UDI
Primary DI / UDI-DI
05060500090012 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Multiple clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple clinical chemistry analyser IVD, laboratory

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

Similar devices

Also classified as Multiple clinical chemistry analyser IVD, laboratory.

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 df71be2b-7324-44b9-ad89-f74854ff2597 36 fields · synced Jun 6, 2026