← Back to catalogue

Abuscreen OnLine Barbiturates

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Abuscreen OnLine Barbiturates FDA UDI
Generic Name
Barbiturate IVD, kit, chemiluminescent immunoassay FDA UDI
Model / Reference
20737976122 FDA UDI

Identifiers

Catalog Number
20737976122 FDA UDI
Primary DI / UDI-DI
04015630993468 FDA UDI
510(k) Number
K951595 FDA UDI
FDA Product Code
DIS FDA UDI
GMDN Term
Barbiturate IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3150 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: Barbiturate IVD, kit, chemiluminescent immunoassay

Abuscreen OnLine Barbiturates by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Barbiturate IVD, kit, chemiluminescent immunoassay.

Cleared under the same submission

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 f3e50178-62bf-4c12-af93-e26e347496fd 35 fields · synced May 29, 2026