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Propoxyphene DAU Calibrator, High Calibrator

FDA UDI

Class II (US FDA UDI)

by Lin-Zhi International, Inc.

Identity

Trade Name
Propoxyphene DAU Calibrator, High Calibrator FDA UDI
Generic Name
Propoxyphene IVD, calibrator FDA UDI
Device Name
5mL/bottle. Concentration: 1000 ng/mL of Propoxyphene. FDA UDI
Model / Reference
0125 FDA UDI
Description
5mL/bottle. Concentration: 1000 ng/mL of Propoxyphene. FDA UDI

Identifiers

Catalog Number
0125 FDA UDI
Primary DI / UDI-DI
B07601250 FDA UDI
510(k) Number
K023316 FDA UDI
FDA Product Code
DLJ FDA UDI
GMDN Term
Propoxyphene IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Propoxyphene IVD, calibrator

Propoxyphene DAU Calibrator, High Calibrator by Lin-Zhi International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Propoxyphene IVD, calibrator.

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 4972c5c8-2613-48f2-a4c5-5ab0e0c262af 36 fields · synced Jun 9, 2026