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Q.E.D. Saliva Alcohol Test A150

FDA UDI

Class II (US FDA UDI)

by OraSure Technologies, Inc.

Identity

Trade Name
Q.E.D. Saliva Alcohol Test A150 FDA UDI
Generic Name
Ethanol (ETOH) IVD, kit, rapid colorimetric, clinical FDA UDI
Model / Reference
60156 FDA UDI

Identifiers

Primary DI / UDI-DI
00608337150308 FDA UDI
510(k) Number
K894001 FDA UDI
FDA Product Code
DIC FDA UDI
GMDN Term
Ethanol (ETOH) IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Ethanol (ETOH) IVD, kit, rapid colorimetric, clinical

Q.E.D. Saliva Alcohol Test A150 by OraSure Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ethanol (ETOH) IVD, kit, rapid colorimetric, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa00af4a-fb3f-4f02-b005-4a9e06ae4d48 35 fields · synced Jun 9, 2026