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POINTE SCIENTIFIC Cholesterol (Liquid)

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
POINTE SCIENTIFIC Cholesterol (Liquid) FDA UDI
Generic Name
Total cholesterol lipid IVD, kit, spectrophotometry FDA UDI
Device Name
For the quantitative determination of Total Cholesterol in serum. FDA UDI
Model / Reference
C7510-120 FDA UDI
Description
For the quantitative determination of Total Cholesterol in serum. FDA UDI

Identifiers

Catalog Number
C7510-120 FDA UDI
Primary DI / UDI-DI
00811727010827 FDA UDI
FDA Product Code
CHH FDA UDI
GMDN Term
Total cholesterol lipid IVD, kit, spectrophotometry 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, kit, spectrophotometry

POINTE SCIENTIFIC Cholesterol (Liquid) 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, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c30f968-8923-4189-9ce6-3d5c76a8fbd8 36 fields · synced Jun 8, 2026