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Oxycodone 100 DAU Control, Level 1 Control

FDA UDI

Class I (US FDA UDI)

by Lin-Zhi International, Inc.

Identity

Trade Name
Oxycodone 100 DAU Control, Level 1 Control FDA UDI
Generic Name
Oxycodone IVD, control FDA UDI
Device Name
5mL/bottle. Concentration: 75 ng/mL of Oxycodone. FDA UDI
Model / Reference
0242b FDA UDI
Description
5mL/bottle. Concentration: 75 ng/mL of Oxycodone. FDA UDI

Identifiers

Catalog Number
0242b FDA UDI
Primary DI / UDI-DI
B0760242B0 FDA UDI
510(k) Number
K120763 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Oxycodone IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 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

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: Oxycodone IVD, control

Oxycodone 100 DAU Control, Level 1 Control by Lin-Zhi International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxycodone 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 0d4831eb-ca7f-41a6-98d0-4a5f67ba8c9d 36 fields · synced Jun 9, 2026