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Barbiturate DAU Calibrator/Control, Calibrator #3/Cutoff A/Control 2

FDA UDI

Class I (US FDA UDI)

by Lin-Zhi International, Inc.

Identity

Trade Name
Barbiturate DAU Calibrator/Control, Calibrator #3/Cutoff A/Control 2 FDA UDI
Generic Name
Barbiturate IVD, control FDA UDI
Device Name
5mL/bottle. Concentration: 200 ng/mL of Secobarbital. FDA UDI
Model / Reference
0143 FDA UDI
Description
5mL/bottle. Concentration: 200 ng/mL of Secobarbital. FDA UDI

Identifiers

Catalog Number
0143 FDA UDI
Primary DI / UDI-DI
B07601430 FDA UDI
510(k) Number
K032764 FDA UDI
FDA Product Code
LAS FDA UDI
DLJ FDA UDI
GMDN Term
Barbiturate IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 FDA UDI
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

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: Barbiturate IVD, calibratorBarbiturate IVD, control

Barbiturate DAU Calibrator/Control, Calibrator #3/Cutoff A/Control 2 by Lin-Zhi International, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Barbiturate IVD, control.

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 cb21d571-4a52-43ee-ae03-7e3cfa044d56 36 fields · synced Jun 9, 2026