← Back to catalogue

Pointe Scientific, Inc.

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. FDA UDI
Generic Name
High density lipoprotein (HDL) cholesterol IVD, calibrator FDA UDI
Device Name
Reagent for the calibration of Pointe Scientific’s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only. 1 x 3ml FDA UDI
Model / Reference
H7545-CAL FDA UDI
Description
Reagent for the calibration of Pointe Scientific’s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only. 1 x 3ml FDA UDI

Identifiers

Catalog Number
H7545-CAL FDA UDI
Primary DI / UDI-DI
00811727011411 FDA UDI
FDA Product Code
LBR FDA UDI
GMDN Term
High density lipoprotein (HDL) cholesterol IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1475 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: High density lipoprotein (HDL) cholesterol 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 High density lipoprotein (HDL) cholesterol IVD, calibrator.

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 0b892b29-6e93-44b8-b490-b49b458706d6 36 fields · synced May 30, 2026