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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
Ethanol (ETOH) IVD, calibrator FDA UDI
Device Name
Alcohol Standards and Controls 6 X 25 mL FDA UDI
Model / Reference
IR952-ETOH FDA UDI
Description
Alcohol Standards and Controls 6 X 25 mL FDA UDI

Identifiers

Catalog Number
IR952-ETOH FDA UDI
Primary DI / UDI-DI
05060500091606 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Ethanol (ETOH) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

Yes

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: Ethanol (ETOH) 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 Ethanol (ETOH) IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b8c199ae-39c5-4ed2-ac74-c4e5263a9b2a 36 fields · synced May 30, 2026