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Pointe Scientific, Inc.

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. FDA UDI
Generic Name
Total cholesterol lipid IVD, calibrator FDA UDI
Device Name
Reagent intended for use as an cholesterol standard for standardization or calibration of enzymatic, endpoint cholesterol procedures. 1 x 200 mg/dl FDA UDI
Model / Reference
13-C7509-STD FDA UDI
Description
Reagent intended for use as an cholesterol standard for standardization or calibration of enzymatic, endpoint cholesterol procedures. 1 x 200 mg/dl FDA UDI

Identifiers

Catalog Number
13-C7509-STD FDA UDI
Primary DI / UDI-DI
00811727013996 FDA UDI
FDA Product Code
CHH FDA UDI
GMDN Term
Total cholesterol lipid IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1175 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total cholesterol lipid IVD, calibrator

Pointe Scientific, Inc. by Pointe Scientific, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total cholesterol lipid IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f83285c9-c9ff-449c-b7de-cc52f98d305a 36 fields · synced May 30, 2026